Canonical Allele Identifier: CA2323005404

Gene: ACP5 ZNF627

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11576104_11576105delinsAG , CM000681.2:g.11576104_11576105delinsAG	GRCh38
NC_000019.9:g.11686919_11686920delinsAG , CM000681.1:g.11686919_11686920delinsAG	GRCh37
NC_000019.8:g.11547919_11547920delinsAG	NCBI36
NG_028127.1:g.7882_7883delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218758.10:c.735+138_735+139delinsCT (ACP5)	ENSP00000218758.4:n.735+138_735+139delinsCT
ENST00000412435.7:c.735+138_735+139delinsCT (ACP5)	ENSP00000392374.1:n.735+138_735+139delinsCT
ENST00000588524.6:n.1368+138_1368+139delinsCT (ACP5)
ENST00000589792.6:c.735+138_735+139delinsCT (ACP5)	ENSP00000468685.2:n.735+138_735+139delinsCT
ENST00000590832.2:c.735+138_735+139delinsCT (ACP5)	ENSP00000465127.2:n.735+138_735+139delinsCT
ENST00000591319.2:c.735+138_735+139delinsCT (ACP5)	ENSP00000464831.2:n.735+138_735+139delinsCT
ENST00000592659.2:c.735+138_735+139delinsCT (ACP5)	ENSP00000465498.2:n.735+138_735+139delinsCT
ENST00000592828.7:c.735+138_735+139delinsCT (ACP5)	ENSP00000468767.3:n.735+138_735+139delinsCT
ENST00000649386.2:c.735+138_735+139delinsCT (ACP5)	ENSP00000497140.2:n.735+138_735+139delinsCT
ENST00000695791.1:c.735+138_735+139delinsCT (ACP5)	ENSP00000512173.1:n.735+138_735+139delinsCT
ENST00000695809.1:c.732+138_732+139delinsCT (ACP5)	ENSP00000512189.1:n.732+138_732+139delinsCT
ENST00000695810.1:c.657+138_657+139delinsCT (ACP5)	ENSP00000512190.1:n.657+138_657+139delinsCT
ENST00000695811.1:c.735+138_735+139delinsCT (ACP5)	ENSP00000512191.1:n.735+138_735+139delinsCT
ENST00000695812.1:n.1353+138_1353+139delinsCT (ACP5)
ENST00000695813.1:c.732+138_732+139delinsCT (ACP5)	ENSP00000512192.1:n.732+138_732+139delinsCT
ENST00000695814.1:c.636+138_636+139delinsCT (ACP5)	ENSP00000512193.1:n.636+138_636+139delinsCT
ENST00000695815.1:c.732+138_732+139delinsCT (ACP5)	ENSP00000512194.1:n.732+138_732+139delinsCT
ENST00000695816.1:n.1290+138_1290+139delinsCT (ACP5)
ENST00000695817.1:c.732+138_732+139delinsCT (ACP5)	ENSP00000512195.1:n.732+138_732+139delinsCT
ENST00000695818.1:c.*238+138_*238+139delinsCT (ACP5)	ENSP00000512196.1:n.*238+138_*238+139delinsCT
ENST00000695819.1:n.1240+138_1240+139delinsCT (ACP5)
ENST00000695820.1:c.657+138_657+139delinsCT (ACP5)	ENSP00000512198.1:n.657+138_657+139delinsCT
ENST00000695821.1:c.657+138_657+139delinsCT (ACP5)	ENSP00000512199.1:n.657+138_657+139delinsCT
ENST00000695838.1:n.2711+138_2711+139delinsCT (ACP5)
ENST00000648477.1:c.735+138_735+139delinsCT (ACP5) MANE Select	ENSP00000496973.1:n.735+138_735+139delinsCT
ENST00000218758.9:c.735+138_735+139delinsCT (ACP5)	ENSP00000218758.4:n.735+138_735+139delinsCT
ENST00000412435.6:c.735+138_735+139delinsCT (ACP5)	ENSP00000392374.1:n.735+138_735+139delinsCT
ENST00000433365.2:c.735+138_735+139delinsCT (ACP5)	ENSP00000413456.1:n.735+138_735+139delinsCT
ENST00000585493.5:c.-94+751_-94+752delinsAG (ZNF627)	ENSP00000464997.1:n.-94+751_-94+752delinsAG
ENST00000590420.1:c.55-899_55-898delinsCT (ACP5)	ENSP00000468509.1:n.55-899_55-898delinsCT
ENST00000592828.5:c.735+138_735+139delinsCT (ACP5)	ENSP00000468767.1:n.735+138_735+139delinsCT
ENST00000593279.5:n.519+751_519+752delinsAG (ZNF627)
NM_001111034.1:c.735+138_735+139delinsCT (ACP5)	NP_001104504.1:n.735+138_735+139delinsCT
NM_001111035.1:c.735+138_735+139delinsCT (ACP5)	NP_001104505.1:n.735+138_735+139delinsCT
NM_001111036.1:c.735+138_735+139delinsCT (ACP5)	NP_001104506.1:n.735+138_735+139delinsCT
NM_001611.3:c.735+138_735+139delinsCT (ACP5)	NP_001602.1:n.735+138_735+139delinsCT
XM_005259938.1:c.735+138_735+139delinsCT (ACP5)	XP_005259995.1:n.735+138_735+139delinsCT
XM_005259939.3:c.735+138_735+139delinsCT (ACP5)	XP_005259996.1:n.735+138_735+139delinsCT
XM_011527780.1:c.-94+751_-94+752delinsAG (ZNF627)	XP_011526082.1:n.-94+751_-94+752delinsAG
XM_011528069.1:c.735+138_735+139delinsCT (ACP5)	XP_011526371.1:n.735+138_735+139delinsCT
NM_001111034.2:c.735+138_735+139delinsCT (ACP5)	NP_001104504.1:n.735+138_735+139delinsCT
NM_001111035.2:c.735+138_735+139delinsCT (ACP5)	NP_001104505.1:n.735+138_735+139delinsCT
NM_001111036.2:c.735+138_735+139delinsCT (ACP5)	NP_001104506.1:n.735+138_735+139delinsCT
NM_001322023.1:c.735+138_735+139delinsCT (ACP5)	NP_001308952.1:n.735+138_735+139delinsCT
NM_001611.5:c.735+138_735+139delinsCT (ACP5) MANE Select	NP_001602.1:n.735+138_735+139delinsCT
XM_011527780.2:c.-94+751_-94+752delinsAG (ZNF627)	XP_011526082.1:n.-94+751_-94+752delinsAG
XM_011528069.2:c.735+138_735+139delinsCT (ACP5)	XP_011526371.1:n.735+138_735+139delinsCT
NM_001111034.3:c.735+138_735+139delinsCT (ACP5)	NP_001104504.1:n.735+138_735+139delinsCT
NM_001111035.3:c.735+138_735+139delinsCT (ACP5)	NP_001104505.1:n.735+138_735+139delinsCT
NM_001111036.3:c.735+138_735+139delinsCT (ACP5)	NP_001104506.1:n.735+138_735+139delinsCT
NM_001322023.2:c.735+138_735+139delinsCT (ACP5)	NP_001308952.1:n.735+138_735+139delinsCT