Canonical Allele Identifier: CA1327160298

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214978776A= , CM000664.2:g.214978776A=	GRCh38
NC_000002.11:g.215843500A= , CM000664.1:g.215843500A=	GRCh37
NC_000002.10:g.215551745A=	NCBI36
NG_007074.1:g.164652T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.4977+28T= MANE Select	ENSP00000272895.7:n.4977+28T=
ENST00000272895.11:c.4977+28T=	ENSP00000272895.7:n.4977+28T=
ENST00000389661.4:c.4023+28T=	ENSP00000374312.4:n.4023+28T=
NM_015657.3:c.4023+28T=	NP_056472.2:n.4023+28T=
NM_173076.2:c.4977+28T=	NP_775099.2:n.4977+28T=
NR_103740.1:n.5277+28T=
XM_011510951.1:c.4986+28T=	XP_011509253.1:n.4986+28T=
XM_011510952.1:c.4986+28T=	XP_011509254.1:n.4986+28T=
XM_011510951.2:c.4986+28T=	XP_011509253.1:n.4986+28T=
NM_173076.3:c.4977+28T= MANE Select	NP_775099.2:n.4977+28T=
NR_103740.2:n.5475+28T=
NM_015657.4:c.4023+28T=	NP_056472.2:n.4023+28T=