Canonical Allele Identifier: CA1327177478

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215019506T= , CM000664.2:g.215019506T=	GRCh38
NC_000002.11:g.215884230T= , CM000664.1:g.215884230T=	GRCh37
NC_000002.10:g.215592475T=	NCBI36
NG_007074.1:g.123922A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.1544+34A= MANE Select	ENSP00000272895.7:n.1544+34A=
ENST00000272895.11:c.1544+34A=	ENSP00000272895.7:n.1544+34A=
ENST00000389661.4:c.590+34A=	ENSP00000374312.4:n.590+34A=
NM_015657.3:c.590+34A=	NP_056472.2:n.590+34A=
NM_173076.2:c.1544+34A=	NP_775099.2:n.1544+34A=
NR_103740.1:n.1788+34A=
XM_011510951.1:c.1544+34A=	XP_011509253.1:n.1544+34A=
XM_011510952.1:c.1544+34A=	XP_011509254.1:n.1544+34A=
XM_011510951.2:c.1544+34A=	XP_011509253.1:n.1544+34A=
NM_173076.3:c.1544+34A= MANE Select	NP_775099.2:n.1544+34A=
NR_103740.2:n.1986+34A=
NM_015657.4:c.590+34A=	NP_056472.2:n.590+34A=