Canonical Allele Identifier: CA404146184

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11576284C>A , CM000681.2:g.11576284C>A GRCh38
NC_000019.9:g.11687099C>A , CM000681.1:g.11687099C>A GRCh37
NC_000019.8:g.11548099C>A NCBI36
NG_028127.1:g.7703G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218758.10:c.694G>T (ACP5) ENSP00000218758.4:p.Gly232Trp
ENST00000412435.7:c.694G>T (ACP5) ENSP00000392374.1:p.Gly232Trp
ENST00000588524.6:n.1327G>T (ACP5)
ENST00000589792.6:c.694G>T (ACP5) ENSP00000468685.2:p.Gly232Trp
ENST00000590832.2:c.694G>T (ACP5) ENSP00000465127.2:p.Gly232Trp
ENST00000591319.2:c.694G>T (ACP5) ENSP00000464831.2:p.Gly232Trp
ENST00000592659.2:c.694G>T (ACP5) ENSP00000465498.2:p.Gly232Trp
ENST00000592828.7:c.694G>T (ACP5) ENSP00000468767.3:p.Gly232Trp
ENST00000649386.2:c.694G>T (ACP5) ENSP00000497140.2:p.Gly232Trp
ENST00000695791.1:c.694G>T (ACP5) ENSP00000512173.1:p.Gly232Trp
ENST00000695809.1:c.691G>T (ACP5) ENSP00000512189.1:p.Gly231Trp
ENST00000695810.1:c.616G>T (ACP5) ENSP00000512190.1:p.Gly206Trp
ENST00000695811.1:c.694G>T (ACP5) ENSP00000512191.1:p.Gly232Trp
ENST00000695812.1:n.1312G>T (ACP5)
ENST00000695813.1:c.691G>T (ACP5) ENSP00000512192.1:p.Gly231Trp
ENST00000695814.1:c.595G>T (ACP5) ENSP00000512193.1:p.Gly199Trp
ENST00000695815.1:c.691G>T (ACP5) ENSP00000512194.1:p.Gly231Trp
ENST00000695816.1:n.1249G>T (ACP5)
ENST00000695817.1:c.691G>T (ACP5) ENSP00000512195.1:p.Gly231Trp
ENST00000695818.1:c.*197G>T (ACP5) ENSP00000512196.1:n.*197G>T
ENST00000695819.1:n.1199G>T (ACP5)
ENST00000695820.1:c.616G>T (ACP5) ENSP00000512198.1:p.Gly206Trp
ENST00000695821.1:c.616G>T (ACP5) ENSP00000512199.1:p.Gly206Trp
ENST00000695838.1:n.2670G>T (ACP5)
ENST00000648477.1:c.694G>T (ACP5) MANE Select ENSP00000496973.1:p.Gly232Trp
ENST00000218758.9:c.694G>T (ACP5) ENSP00000218758.4:p.Gly232Trp
ENST00000412435.6:c.694G>T (ACP5) ENSP00000392374.1:p.Gly232Trp
ENST00000433365.2:c.694G>T (ACP5) ENSP00000413456.1:p.Gly232Trp
ENST00000585493.5:c.-94+931C>A (ZNF627) ENSP00000464997.1:n.-94+931C>A
ENST00000590420.1:c.54+980G>T (ACP5) ENSP00000468509.1:n.54+980G>T
ENST00000592828.5:c.694G>T (ACP5) ENSP00000468767.1:p.Gly232Trp
ENST00000593279.5:n.519+931C>A (ZNF627)
NM_001111034.1:c.694G>T (ACP5) NP_001104504.1:p.Gly232Trp
NM_001111035.1:c.694G>T (ACP5) NP_001104505.1:p.Gly232Trp
NM_001111036.1:c.694G>T (ACP5) NP_001104506.1:p.Gly232Trp
NM_001611.3:c.694G>T (ACP5) NP_001602.1:p.Gly232Trp
XM_005259938.1:c.694G>T (ACP5) XP_005259995.1:p.Gly232Trp
XM_005259939.3:c.694G>T (ACP5) XP_005259996.1:p.Gly232Trp
XM_011527780.1:c.-94+931C>A (ZNF627) XP_011526082.1:n.-94+931C>A
XM_011528069.1:c.694G>T (ACP5) XP_011526371.1:p.Gly232Trp
NM_001111034.2:c.694G>T (ACP5) NP_001104504.1:p.Gly232Trp
NM_001111035.2:c.694G>T (ACP5) NP_001104505.1:p.Gly232Trp
NM_001111036.2:c.694G>T (ACP5) NP_001104506.1:p.Gly232Trp
NM_001322023.1:c.694G>T (ACP5) NP_001308952.1:p.Gly232Trp
NM_001611.5:c.694G>T (ACP5) MANE Select NP_001602.1:p.Gly232Trp
XM_011527780.2:c.-94+931C>A (ZNF627) XP_011526082.1:n.-94+931C>A
XM_011528069.2:c.694G>T (ACP5) XP_011526371.1:p.Gly232Trp
NM_001111034.3:c.694G>T (ACP5) NP_001104504.1:p.Gly232Trp
NM_001111035.3:c.694G>T (ACP5) NP_001104505.1:p.Gly232Trp
NM_001111036.3:c.694G>T (ACP5) NP_001104506.1:p.Gly232Trp
NM_001322023.2:c.694G>T (ACP5) NP_001308952.1:p.Gly232Trp