Canonical Allele Identifier: CA1327161028

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980633G= , CM000664.2:g.214980633G=	GRCh38
NC_000002.11:g.215845357G= , CM000664.1:g.215845357G=	GRCh37
NC_000002.10:g.215553602G=	NCBI36
NG_007074.1:g.162795C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.4590C= MANE Select	ENSP00000272895.7:p.Ile1530=
ENST00000272895.11:c.4590C=	ENSP00000272895.7:p.Ile1530=
ENST00000389661.4:c.3636C=	ENSP00000374312.4:p.Ile1212=
NM_015657.3:c.3636C=	NP_056472.2:p.Ile1212=
NM_173076.2:c.4590C=	NP_775099.2:p.Ile1530=
NR_103740.1:n.4890C=
XM_011510951.1:c.4599C=	XP_011509253.1:p.Ile1533=
XM_011510952.1:c.4599C=	XP_011509254.1:p.Ile1533=
XM_011510951.2:c.4599C=	XP_011509253.1:p.Ile1533=
NM_173076.3:c.4590C= MANE Select	NP_775099.2:p.Ile1530=
NR_103740.2:n.5088C=
NM_015657.4:c.3636C=	NP_056472.2:p.Ile1212=