Canonical Allele Identifier: CA1327147229

Gene: ABCA12 SNHG31

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214947402T= , CM000664.2:g.214947402T=	GRCh38
NC_000002.11:g.215812126T= , CM000664.1:g.215812126T=	GRCh37
NC_000002.10:g.215520371T=	NCBI36
NG_007074.1:g.196026A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.7239+20A= (ABCA12) MANE Select	ENSP00000272895.7:n.7239+20A=
ENST00000272895.11:c.7239+20A= (ABCA12)	ENSP00000272895.7:n.7239+20A=
ENST00000389661.4:c.6285+20A= (ABCA12)	ENSP00000374312.4:n.6285+20A=
NM_015657.3:c.6285+20A= (ABCA12)	NP_056472.2:n.6285+20A=
NM_173076.2:c.7239+20A= (ABCA12)	NP_775099.2:n.7239+20A=
NR_103740.1:n.7539+20A= (ABCA12)
NR_110292.1:n.322-423T= (SNHG31)
XM_011510951.1:c.7248+20A= (ABCA12)	XP_011509253.1:n.7248+20A=
XM_011510951.2:c.7248+20A= (ABCA12)	XP_011509253.1:n.7248+20A=
NM_173076.3:c.7239+20A= (ABCA12) MANE Select	NP_775099.2:n.7239+20A=
NR_103740.2:n.7737+20A= (ABCA12)
NM_015657.4:c.6285+20A= (ABCA12)	NP_056472.2:n.6285+20A=