Canonical Allele Identifier: CA1327174226

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011741G= , CM000664.2:g.215011741G=	GRCh38
NC_000002.11:g.215876465G= , CM000664.1:g.215876465G=	GRCh37
NC_000002.10:g.215584710G=	NCBI36
NG_007074.1:g.131687C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.2122-92C= MANE Select	ENSP00000272895.7:n.2122-92C=
ENST00000272895.11:c.2122-92C=	ENSP00000272895.7:n.2122-92C=
ENST00000389661.4:c.1168-92C=	ENSP00000374312.4:n.1168-92C=
NM_015657.3:c.1168-92C=	NP_056472.2:n.1168-92C=
NM_173076.2:c.2122-92C=	NP_775099.2:n.2122-92C=
NR_103740.1:n.2366-92C=
XM_011510951.1:c.2122-92C=	XP_011509253.1:n.2122-92C=
XM_011510952.1:c.2122-92C=	XP_011509254.1:n.2122-92C=
XM_011510951.2:c.2122-92C=	XP_011509253.1:n.2122-92C=
NM_173076.3:c.2122-92C= MANE Select	NP_775099.2:n.2122-92C=
NR_103740.2:n.2564-92C=
NM_015657.4:c.1168-92C=	NP_056472.2:n.1168-92C=