Canonical Allele Identifier: CA350458852
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064214G>T , CM000664.2:g.215064214G>T GRCh38
NC_000002.11:g.215928937G>T , CM000664.1:g.215928937G>T GRCh37
NC_000002.10:g.215637182G>T NCBI36
NG_007074.1:g.79215C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.169C>A MANE Select ENSP00000272895.7:p.Leu57Ile
ENST00000272895.11:c.169C>A ENSP00000272895.7:p.Leu57Ile
NM_173076.2:c.169C>A NP_775099.2:p.Leu57Ile
NR_103740.1:n.389C>A
XM_011510951.1:c.169C>A XP_011509253.1:p.Leu57Ile
XM_011510952.1:c.169C>A XP_011509254.1:p.Leu57Ile
XM_011510951.2:c.169C>A XP_011509253.1:p.Leu57Ile
NM_173076.3:c.169C>A MANE Select NP_775099.2:p.Leu57Ile
NR_103740.2:n.587C>A