Canonical Allele Identifier: CA1327146119

Gene: ABCA12 SNHG31

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214944856A= , CM000664.2:g.214944856A=	GRCh38
NC_000002.11:g.215809580A= , CM000664.1:g.215809580A=	GRCh37
NC_000002.10:g.215517825A=	NCBI36
NG_007074.1:g.198572T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.7343+145T= (ABCA12) MANE Select	ENSP00000272895.7:n.7343+145T=
ENST00000272895.11:c.7343+145T= (ABCA12)	ENSP00000272895.7:n.7343+145T=
ENST00000389661.4:c.6389+145T= (ABCA12)	ENSP00000374312.4:n.6389+145T=
NM_015657.3:c.6389+145T= (ABCA12)	NP_056472.2:n.6389+145T=
NM_173076.2:c.7343+145T= (ABCA12)	NP_775099.2:n.7343+145T=
NR_103740.1:n.7643+145T= (ABCA12)
NR_110292.1:n.322-2969A= (SNHG31)
XM_011510951.1:c.7352+145T= (ABCA12)	XP_011509253.1:n.7352+145T=
XM_011510951.2:c.7352+145T= (ABCA12)	XP_011509253.1:n.7352+145T=
NM_173076.3:c.7343+145T= (ABCA12) MANE Select	NP_775099.2:n.7343+145T=
NR_103740.2:n.7841+145T= (ABCA12)
NM_015657.4:c.6389+145T= (ABCA12)	NP_056472.2:n.6389+145T=