Canonical Allele Identifier: CA1327141138

Gene: ABCA12 SNHG31

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932645T= , CM000664.2:g.214932645T=	GRCh38
NC_000002.11:g.215797369T= , CM000664.1:g.215797369T=	GRCh37
NC_000002.10:g.215505614T=	NCBI36
NG_007074.1:g.210783A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.7777A= (ABCA12) MANE Select	ENSP00000272895.7:p.Met2593=
ENST00000272895.11:c.7777A= (ABCA12)	ENSP00000272895.7:p.Met2593=
ENST00000389661.4:c.6823A= (ABCA12)	ENSP00000374312.4:p.Met2275=
NM_015657.3:c.6823A= (ABCA12)	NP_056472.2:p.Met2275=
NM_173076.2:c.7777A= (ABCA12)	NP_775099.2:p.Met2593=
NR_103740.1:n.8077A= (ABCA12)
NR_110292.1:n.322-15180T= (SNHG31)
XM_011510951.1:c.7786A= (ABCA12)	XP_011509253.1:p.Met2596=
XM_011510951.2:c.7786A= (ABCA12)	XP_011509253.1:p.Met2596=
NM_173076.3:c.7777A= (ABCA12) MANE Select	NP_775099.2:p.Met2593=
NR_103740.2:n.8275A= (ABCA12)
NM_015657.4:c.6823A= (ABCA12)	NP_056472.2:p.Met2275=