Canonical Allele Identifier: CA1327161017

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980600T= , CM000664.2:g.214980600T=	GRCh38
NC_000002.11:g.215845324T= , CM000664.1:g.215845324T=	GRCh37
NC_000002.10:g.215553569T=	NCBI36
NG_007074.1:g.162828A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.4623A= MANE Select	ENSP00000272895.7:p.Glu1541=
ENST00000272895.11:c.4623A=	ENSP00000272895.7:p.Glu1541=
ENST00000389661.4:c.3669A=	ENSP00000374312.4:p.Glu1223=
NM_015657.3:c.3669A=	NP_056472.2:p.Glu1223=
NM_173076.2:c.4623A=	NP_775099.2:p.Glu1541=
NR_103740.1:n.4923A=
XM_011510951.1:c.4632A=	XP_011509253.1:p.Glu1544=
XM_011510952.1:c.4632A=	XP_011509254.1:p.Glu1544=
XM_011510951.2:c.4632A=	XP_011509253.1:p.Glu1544=
NM_173076.3:c.4623A= MANE Select	NP_775099.2:p.Glu1541=
NR_103740.2:n.5121A=
NM_015657.4:c.3669A=	NP_056472.2:p.Glu1223=