Canonical Allele Identifier: CA1327165439

Gene: ABCA12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214991028T= , CM000664.2:g.214991028T=	GRCh38
NC_000002.11:g.215855752T= , CM000664.1:g.215855752T=	GRCh37
NC_000002.10:g.215563997T=	NCBI36
NG_007074.1:g.152400A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.3298A= MANE Select	ENSP00000272895.7:p.Met1100=
ENST00000272895.11:c.3298A=	ENSP00000272895.7:p.Met1100=
ENST00000389661.4:c.2344A=	ENSP00000374312.4:p.Met782=
NM_015657.3:c.2344A=	NP_056472.2:p.Met782=
NM_173076.2:c.3298A=	NP_775099.2:p.Met1100=
NR_103740.1:n.3598A=
XM_011510951.1:c.3298A=	XP_011509253.1:p.Met1100=
XM_011510952.1:c.3298A=	XP_011509254.1:p.Met1100=
XM_011510951.2:c.3298A=	XP_011509253.1:p.Met1100=
NM_173076.3:c.3298A= MANE Select	NP_775099.2:p.Met1100=
NR_103740.2:n.3796A=
NM_015657.4:c.2344A=	NP_056472.2:p.Met782=