Canonical Allele Identifier: CA350458841
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064211C>G , CM000664.2:g.215064211C>G GRCh38
NC_000002.11:g.215928934C>G , CM000664.1:g.215928934C>G GRCh37
NC_000002.10:g.215637179C>G NCBI36
NG_007074.1:g.79218G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.172G>C MANE Select ENSP00000272895.7:p.Ala58Pro
ENST00000272895.11:c.172G>C ENSP00000272895.7:p.Ala58Pro
NM_173076.2:c.172G>C NP_775099.2:p.Ala58Pro
NR_103740.1:n.392G>C
XM_011510951.1:c.172G>C XP_011509253.1:p.Ala58Pro
XM_011510952.1:c.172G>C XP_011509254.1:p.Ala58Pro
XM_011510951.2:c.172G>C XP_011509253.1:p.Ala58Pro
NM_173076.3:c.172G>C MANE Select NP_775099.2:p.Ala58Pro
NR_103740.2:n.590G>C