Canonical Allele Identifier: CA350467975
Community Standard Title: NM_173076.3(ABCA12):c.3656C>T (p.Ala1219Val)
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214989590G>A , CM000664.2:g.214989590G>A GRCh38
NC_000002.11:g.215854314G>A , CM000664.1:g.215854314G>A GRCh37
NC_000002.10:g.215562559G>A NCBI36
NG_007074.1:g.153838C>T

Transcript Alleles

HGVS Amino-acid Change
NM_173076.3:c.3656C>T MANE Select NP_775099.2:p.Ala1219Val
ENST00000272895.12:c.3656C>T MANE Select ENSP00000272895.7:p.Ala1219Val
NM_015657.3:c.2702C>T NP_056472.2:p.Ala901Val
NM_015657.4:c.2702C>T NP_056472.2:p.Ala901Val
NM_173076.2:c.3656C>T NP_775099.2:p.Ala1219Val
NR_103740.1:n.3956C>T
NR_103740.2:n.4154C>T
ENST00000272895.11:c.3656C>T ENSP00000272895.7:p.Ala1219Val
ENST00000389661.4:c.2702C>T ENSP00000374312.4:p.Ala901Val
XM_011510951.1:c.3656C>T XP_011509253.1:p.Ala1219Val
XM_011510951.2:c.3656C>T XP_011509253.1:p.Ala1219Val
XM_011510952.1:c.3656C>T XP_011509254.1:p.Ala1219Val