Canonical Allele Identifier: CA1327174127

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011519C= , CM000664.2:g.215011519C=	GRCh38
NC_000002.11:g.215876243C= , CM000664.1:g.215876243C=	GRCh37
NC_000002.10:g.215584488C=	NCBI36
NG_007074.1:g.131909G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.2252G= MANE Select	ENSP00000272895.7:p.Gly751=
ENST00000272895.11:c.2252G=	ENSP00000272895.7:p.Gly751=
ENST00000389661.4:c.1298G=	ENSP00000374312.4:p.Gly433=
NM_015657.3:c.1298G=	NP_056472.2:p.Gly433=
NM_173076.2:c.2252G=	NP_775099.2:p.Gly751=
NR_103740.1:n.2496G=
XM_011510951.1:c.2252G=	XP_011509253.1:p.Gly751=
XM_011510952.1:c.2252G=	XP_011509254.1:p.Gly751=
XM_011510951.2:c.2252G=	XP_011509253.1:p.Gly751=
NM_173076.3:c.2252G= MANE Select	NP_775099.2:p.Gly751=
NR_103740.2:n.2694G=
NM_015657.4:c.1298G=	NP_056472.2:p.Gly433=