Canonical Allele Identifier: CA1327174079

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011398C= , CM000664.2:g.215011398C=	GRCh38
NC_000002.11:g.215876122C= , CM000664.1:g.215876122C=	GRCh37
NC_000002.10:g.215584367C=	NCBI36
NG_007074.1:g.132030G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.2332+41G= MANE Select	ENSP00000272895.7:n.2332+41G=
ENST00000272895.11:c.2332+41G=	ENSP00000272895.7:n.2332+41G=
ENST00000389661.4:c.1378+41G=	ENSP00000374312.4:n.1378+41G=
NM_015657.3:c.1378+41G=	NP_056472.2:n.1378+41G=
NM_173076.2:c.2332+41G=	NP_775099.2:n.2332+41G=
NR_103740.1:n.2576+41G=
XM_011510951.1:c.2332+41G=	XP_011509253.1:n.2332+41G=
XM_011510952.1:c.2332+41G=	XP_011509254.1:n.2332+41G=
XM_011510951.2:c.2332+41G=	XP_011509253.1:n.2332+41G=
NM_173076.3:c.2332+41G= MANE Select	NP_775099.2:n.2332+41G=
NR_103740.2:n.2774+41G=
NM_015657.4:c.1378+41G=	NP_056472.2:n.1378+41G=