Canonical Allele Identifier: CA9215389

Gene: ACP5 ZNF627

Linked Data

• ClinVar Variation Id: 847141
• ClinVar RCV Id: RCV001050624
• dbSNP Id: rs202169550
• ExAC: 19:11687249 G / A
• gnomAD v2: 19-11687249-G-A
• gnomAD v3: 19-11576434-G-A
• gnomAD v4: 19-11576434-G-A
• MyVariant Identifiers: chr19:g.11687249G>A (hg19) ; chr19:g.11576434G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11576434G>A , CM000681.2:g.11576434G>A	GRCh38
NC_000019.9:g.11687249G>A , CM000681.1:g.11687249G>A	GRCh37
NC_000019.8:g.11548249G>A	NCBI36
NG_028127.1:g.7553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218758.10:c.544C>T (ACP5)	ENSP00000218758.4:p.Arg182Cys
ENST00000412435.7:c.544C>T (ACP5)	ENSP00000392374.1:p.Arg182Cys
ENST00000588524.6:n.1177C>T (ACP5)
ENST00000588625.2:c.669C>T (ACP5)	ENSP00000512197.1:n.669C>T
ENST00000589792.6:c.544C>T (ACP5)	ENSP00000468685.2:p.Arg182Cys
ENST00000590832.2:c.544C>T (ACP5)	ENSP00000465127.2:p.Arg182Cys
ENST00000591319.2:c.544C>T (ACP5)	ENSP00000464831.2:p.Arg182Cys
ENST00000592659.2:c.544C>T (ACP5)	ENSP00000465498.2:p.Arg182Cys
ENST00000592828.7:c.544C>T (ACP5)	ENSP00000468767.3:p.Arg182Cys
ENST00000649386.2:c.544C>T (ACP5)	ENSP00000497140.2:p.Arg182Cys
ENST00000695791.1:c.544C>T (ACP5)	ENSP00000512173.1:p.Arg182Cys
ENST00000695809.1:c.541C>T (ACP5)	ENSP00000512189.1:p.Arg181Cys
ENST00000695810.1:c.466C>T (ACP5)	ENSP00000512190.1:p.Arg156Cys
ENST00000695811.1:c.544C>T (ACP5)	ENSP00000512191.1:p.Arg182Cys
ENST00000695812.1:n.1162C>T (ACP5)
ENST00000695813.1:c.541C>T (ACP5)	ENSP00000512192.1:p.Arg181Cys
ENST00000695814.1:c.445C>T (ACP5)	ENSP00000512193.1:p.Arg149Cys
ENST00000695815.1:c.541C>T (ACP5)	ENSP00000512194.1:p.Arg181Cys
ENST00000695816.1:n.1099C>T (ACP5)
ENST00000695817.1:c.541C>T (ACP5)	ENSP00000512195.1:p.Arg181Cys
ENST00000695818.1:c.*47C>T (ACP5)	ENSP00000512196.1:n.*47C>T
ENST00000695819.1:n.1049C>T (ACP5)
ENST00000695820.1:c.466C>T (ACP5)	ENSP00000512198.1:p.Arg156Cys
ENST00000695821.1:c.466C>T (ACP5)	ENSP00000512199.1:p.Arg156Cys
ENST00000695838.1:n.2520C>T (ACP5)
ENST00000648477.1:c.544C>T (ACP5) MANE Select	ENSP00000496973.1:p.Arg182Cys
ENST00000218758.9:c.544C>T (ACP5)	ENSP00000218758.4:p.Arg182Cys
ENST00000412435.6:c.544C>T (ACP5)	ENSP00000392374.1:p.Arg182Cys
ENST00000433365.2:c.544C>T (ACP5)	ENSP00000413456.1:p.Arg182Cys
ENST00000585493.5:c.-94+1081G>A (ZNF627)	ENSP00000464997.1:n.-94+1081G>A
ENST00000588625.1:n.383C>T (ACP5)
ENST00000590420.1:c.54+830C>T (ACP5)	ENSP00000468509.1:n.54+830C>T
ENST00000592828.5:c.544C>T (ACP5)	ENSP00000468767.1:p.Arg182Cys
ENST00000593279.5:n.519+1081G>A (ZNF627)
NM_001111034.1:c.544C>T (ACP5)	NP_001104504.1:p.Arg182Cys
NM_001111035.1:c.544C>T (ACP5)	NP_001104505.1:p.Arg182Cys
NM_001111036.1:c.544C>T (ACP5)	NP_001104506.1:p.Arg182Cys
NM_001611.3:c.544C>T (ACP5)	NP_001602.1:p.Arg182Cys
XM_005259938.1:c.544C>T (ACP5)	XP_005259995.1:p.Arg182Cys
XM_005259939.3:c.544C>T (ACP5)	XP_005259996.1:p.Arg182Cys
XM_011527780.1:c.-94+1081G>A (ZNF627)	XP_011526082.1:n.-94+1081G>A
XM_011528069.1:c.544C>T (ACP5)	XP_011526371.1:p.Arg182Cys
NM_001111034.2:c.544C>T (ACP5)	NP_001104504.1:p.Arg182Cys
NM_001111035.2:c.544C>T (ACP5)	NP_001104505.1:p.Arg182Cys
NM_001111036.2:c.544C>T (ACP5)	NP_001104506.1:p.Arg182Cys
NM_001322023.1:c.544C>T (ACP5)	NP_001308952.1:p.Arg182Cys
NM_001611.5:c.544C>T (ACP5) MANE Select	NP_001602.1:p.Arg182Cys
XM_011527780.2:c.-94+1081G>A (ZNF627)	XP_011526082.1:n.-94+1081G>A
XM_011528069.2:c.544C>T (ACP5)	XP_011526371.1:p.Arg182Cys
NM_001111034.3:c.544C>T (ACP5)	NP_001104504.1:p.Arg182Cys
NM_001111035.3:c.544C>T (ACP5)	NP_001104505.1:p.Arg182Cys
NM_001111036.3:c.544C>T (ACP5)	NP_001104506.1:p.Arg182Cys
NM_001322023.2:c.544C>T (ACP5)	NP_001308952.1:p.Arg182Cys