Canonical Allele Identifier: CA1327150011

Gene: ABCA12 SNHG31

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214953776A= , CM000664.2:g.214953776A=	GRCh38
NC_000002.11:g.215818500A= , CM000664.1:g.215818500A=	GRCh37
NC_000002.10:g.215526745A=	NCBI36
NG_007074.1:g.189652T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.6647+78T= (ABCA12) MANE Select	ENSP00000272895.7:n.6647+78T=
ENST00000272895.11:c.6647+78T= (ABCA12)	ENSP00000272895.7:n.6647+78T=
ENST00000389661.4:c.5693+78T= (ABCA12)	ENSP00000374312.4:n.5693+78T=
NM_015657.3:c.5693+78T= (ABCA12)	NP_056472.2:n.5693+78T=
NM_173076.2:c.6647+78T= (ABCA12)	NP_775099.2:n.6647+78T=
NR_103740.1:n.6947+78T= (ABCA12)
NR_110292.1:n.444+5829A= (SNHG31)
XM_011510951.1:c.6656+78T= (ABCA12)	XP_011509253.1:n.6656+78T=
XM_011510951.2:c.6656+78T= (ABCA12)	XP_011509253.1:n.6656+78T=
NM_173076.3:c.6647+78T= (ABCA12) MANE Select	NP_775099.2:n.6647+78T=
NR_103740.2:n.7145+78T= (ABCA12)
NM_015657.4:c.5693+78T= (ABCA12)	NP_056472.2:n.5693+78T=