Canonical Allele Identifier: CA1327140800

Gene: ABCA12 SNHG31

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932335A= , CM000664.2:g.214932335A=	GRCh38
NC_000002.11:g.215797059A= , CM000664.1:g.215797059A=	GRCh37
NC_000002.10:g.215505304A=	NCBI36
NG_007074.1:g.211093T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.*299T= (ABCA12) MANE Select	ENSP00000272895.7:n.*299T=
ENST00000272895.11:c.*299T= (ABCA12)	ENSP00000272895.7:n.*299T=
NM_015657.3:c.*299T= (ABCA12)	NP_056472.2:n.*299T=
NM_173076.2:c.*299T= (ABCA12)	NP_775099.2:n.*299T=
NR_103740.1:n.8387T= (ABCA12)
NR_110292.1:n.322-15490A= (SNHG31)
XM_011510951.1:c.*299T= (ABCA12)	XP_011509253.1:n.*299T=
XM_011510951.2:c.*299T= (ABCA12)	XP_011509253.1:n.*299T=
NM_173076.3:c.*299T= (ABCA12) MANE Select	NP_775099.2:n.*299T=
NR_103740.2:n.8585T= (ABCA12)
NM_015657.4:c.*299T= (ABCA12)	NP_056472.2:n.*299T=