Canonical Allele Identifier: CA1327197010
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064205G= , CM000664.2:g.215064205G= GRCh38
NC_000002.11:g.215928928G= , CM000664.1:g.215928928G= GRCh37
NC_000002.10:g.215637173G= NCBI36
NG_007074.1:g.79224C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.178C= MANE Select ENSP00000272895.7:p.Arg60=
ENST00000272895.11:c.178C= ENSP00000272895.7:p.Arg60=
NM_173076.2:c.178C= NP_775099.2:p.Arg60=
NR_103740.1:n.398C=
XM_011510951.1:c.178C= XP_011509253.1:p.Arg60=
XM_011510952.1:c.178C= XP_011509254.1:p.Arg60=
XM_011510951.2:c.178C= XP_011509253.1:p.Arg60=
NM_173076.3:c.178C= MANE Select NP_775099.2:p.Arg60=
NR_103740.2:n.596C=