Canonical Allele Identifier: CA1327161022

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980616T= , CM000664.2:g.214980616T=	GRCh38
NC_000002.11:g.215845340T= , CM000664.1:g.215845340T=	GRCh37
NC_000002.10:g.215553585T=	NCBI36
NG_007074.1:g.162812A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.4607A= MANE Select	ENSP00000272895.7:p.His1536=
ENST00000272895.11:c.4607A=	ENSP00000272895.7:p.His1536=
ENST00000389661.4:c.3653A=	ENSP00000374312.4:p.His1218=
NM_015657.3:c.3653A=	NP_056472.2:p.His1218=
NM_173076.2:c.4607A=	NP_775099.2:p.His1536=
NR_103740.1:n.4907A=
XM_011510951.1:c.4616A=	XP_011509253.1:p.His1539=
XM_011510952.1:c.4616A=	XP_011509254.1:p.His1539=
XM_011510951.2:c.4616A=	XP_011509253.1:p.His1539=
NM_173076.3:c.4607A= MANE Select	NP_775099.2:p.His1536=
NR_103740.2:n.5105A=
NM_015657.4:c.3653A=	NP_056472.2:p.His1218=