Canonical Allele Identifier: CA1327177502

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215019572T= , CM000664.2:g.215019572T=	GRCh38
NC_000002.11:g.215884296T= , CM000664.1:g.215884296T=	GRCh37
NC_000002.10:g.215592541T=	NCBI36
NG_007074.1:g.123856A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.1512A= MANE Select	ENSP00000272895.7:p.Gly504=
ENST00000272895.11:c.1512A=	ENSP00000272895.7:p.Gly504=
ENST00000389661.4:c.558A=	ENSP00000374312.4:p.Gly186=
NM_015657.3:c.558A=	NP_056472.2:p.Gly186=
NM_173076.2:c.1512A=	NP_775099.2:p.Gly504=
NR_103740.1:n.1756A=
XM_011510951.1:c.1512A=	XP_011509253.1:p.Gly504=
XM_011510952.1:c.1512A=	XP_011509254.1:p.Gly504=
XM_011510951.2:c.1512A=	XP_011509253.1:p.Gly504=
NM_173076.3:c.1512A= MANE Select	NP_775099.2:p.Gly504=
NR_103740.2:n.1954A=
NM_015657.4:c.558A=	NP_056472.2:p.Gly186=