Canonical Allele Identifier: CA350460742
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214980508T>C , CM000664.2:g.214980508T>C GRCh38
NC_000002.11:g.215845232T>C , CM000664.1:g.215845232T>C GRCh37
NC_000002.10:g.215553477T>C NCBI36
NG_007074.1:g.162920A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.4715A>G MANE Select ENSP00000272895.7:p.Tyr1572Cys
ENST00000272895.11:c.4715A>G ENSP00000272895.7:p.Tyr1572Cys
ENST00000389661.4:c.3761A>G ENSP00000374312.4:p.Tyr1254Cys
NM_015657.3:c.3761A>G NP_056472.2:p.Tyr1254Cys
NM_173076.2:c.4715A>G NP_775099.2:p.Tyr1572Cys
NR_103740.1:n.5015A>G
XM_011510951.1:c.4724A>G XP_011509253.1:p.Tyr1575Cys
XM_011510952.1:c.4724A>G XP_011509254.1:p.Tyr1575Cys
XM_011510951.2:c.4724A>G XP_011509253.1:p.Tyr1575Cys
NM_173076.3:c.4715A>G MANE Select NP_775099.2:p.Tyr1572Cys
NR_103740.2:n.5213A>G
NM_015657.4:c.3761A>G NP_056472.2:p.Tyr1254Cys