Canonical Allele Identifier: CA1327177549

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215019691C= , CM000664.2:g.215019691C=	GRCh38
NC_000002.11:g.215884415C= , CM000664.1:g.215884415C=	GRCh37
NC_000002.10:g.215592660C=	NCBI36
NG_007074.1:g.123737G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.1393G= MANE Select	ENSP00000272895.7:p.Glu465=
ENST00000272895.11:c.1393G=	ENSP00000272895.7:p.Glu465=
ENST00000389661.4:c.439G=	ENSP00000374312.4:p.Glu147=
NM_015657.3:c.439G=	NP_056472.2:p.Glu147=
NM_173076.2:c.1393G=	NP_775099.2:p.Glu465=
NR_103740.1:n.1637G=
XM_011510951.1:c.1393G=	XP_011509253.1:p.Glu465=
XM_011510952.1:c.1393G=	XP_011509254.1:p.Glu465=
XM_011510951.2:c.1393G=	XP_011509253.1:p.Glu465=
NM_173076.3:c.1393G= MANE Select	NP_775099.2:p.Glu465=
NR_103740.2:n.1835G=
NM_015657.4:c.439G=	NP_056472.2:p.Glu147=