Canonical Allele Identifier: CA1327174228

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011744T= , CM000664.2:g.215011744T=	GRCh38
NC_000002.11:g.215876468T= , CM000664.1:g.215876468T=	GRCh37
NC_000002.10:g.215584713T=	NCBI36
NG_007074.1:g.131684A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.2122-95A= MANE Select	ENSP00000272895.7:n.2122-95A=
ENST00000272895.11:c.2122-95A=	ENSP00000272895.7:n.2122-95A=
ENST00000389661.4:c.1168-95A=	ENSP00000374312.4:n.1168-95A=
NM_015657.3:c.1168-95A=	NP_056472.2:n.1168-95A=
NM_173076.2:c.2122-95A=	NP_775099.2:n.2122-95A=
NR_103740.1:n.2366-95A=
XM_011510951.1:c.2122-95A=	XP_011509253.1:n.2122-95A=
XM_011510952.1:c.2122-95A=	XP_011509254.1:n.2122-95A=
XM_011510951.2:c.2122-95A=	XP_011509253.1:n.2122-95A=
NM_173076.3:c.2122-95A= MANE Select	NP_775099.2:n.2122-95A=
NR_103740.2:n.2564-95A=
NM_015657.4:c.1168-95A=	NP_056472.2:n.1168-95A=