Canonical Allele Identifier: CA1327140690

Gene: ABCA12 SNHG31

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932228C= , CM000664.2:g.214932228C=	GRCh38
NC_000002.11:g.215796952C= , CM000664.1:g.215796952C=	GRCh37
NC_000002.10:g.215505197C=	NCBI36
NG_007074.1:g.211200G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.*406G= (ABCA12) MANE Select	ENSP00000272895.7:n.*406G=
ENST00000272895.11:c.*406G= (ABCA12)	ENSP00000272895.7:n.*406G=
NM_015657.3:c.*406G= (ABCA12)	NP_056472.2:n.*406G=
NM_173076.2:c.*406G= (ABCA12)	NP_775099.2:n.*406G=
NR_103740.1:n.8494G= (ABCA12)
NR_110292.1:n.322-15597C= (SNHG31)
XM_011510951.1:c.*406G= (ABCA12)	XP_011509253.1:n.*406G=
XM_011510951.2:c.*406G= (ABCA12)	XP_011509253.1:n.*406G=
NM_173076.3:c.*406G= (ABCA12) MANE Select	NP_775099.2:n.*406G=
NR_103740.2:n.8692G= (ABCA12)
NM_015657.4:c.*406G= (ABCA12)	NP_056472.2:n.*406G=