Canonical Allele Identifier: CA1327172827

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011969A= , CM000664.2:g.215011969A=	GRCh38
NC_000002.11:g.215876693A= , CM000664.1:g.215876693A=	GRCh37
NC_000002.10:g.215584938A=	NCBI36
NG_007074.1:g.131459T=

Transcript Alleles

HGVS	Amino-acid Change
NM_173076.3:c.2121+2T= MANE Select	NP_775099.2:n.2121+2T=
ENST00000272895.12:c.2121+2T= MANE Select	ENSP00000272895.7:n.2121+2T=
NM_015657.3:c.1167+2T=	NP_056472.2:n.1167+2T=
NM_015657.4:c.1167+2T=	NP_056472.2:n.1167+2T=
NM_173076.2:c.2121+2T=	NP_775099.2:n.2121+2T=
NR_103740.1:n.2365+2T=
NR_103740.2:n.2563+2T=
ENST00000272895.11:c.2121+2T=	ENSP00000272895.7:n.2121+2T=
ENST00000389661.4:c.1167+2T=	ENSP00000374312.4:n.1167+2T=
XM_011510951.1:c.2121+2T=	XP_011509253.1:n.2121+2T=
XM_011510951.2:c.2121+2T=	XP_011509253.1:n.2121+2T=
XM_011510952.1:c.2121+2T=	XP_011509254.1:n.2121+2T=