Canonical Allele Identifier: CA1327146185

Gene: ABCA12 SNHG31

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214944970G= , CM000664.2:g.214944970G=	GRCh38
NC_000002.11:g.215809694G= , CM000664.1:g.215809694G=	GRCh37
NC_000002.10:g.215517939G=	NCBI36
NG_007074.1:g.198458C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.7343+31C= (ABCA12) MANE Select	ENSP00000272895.7:n.7343+31C=
ENST00000272895.11:c.7343+31C= (ABCA12)	ENSP00000272895.7:n.7343+31C=
ENST00000389661.4:c.6389+31C= (ABCA12)	ENSP00000374312.4:n.6389+31C=
NM_015657.3:c.6389+31C= (ABCA12)	NP_056472.2:n.6389+31C=
NM_173076.2:c.7343+31C= (ABCA12)	NP_775099.2:n.7343+31C=
NR_103740.1:n.7643+31C= (ABCA12)
NR_110292.1:n.322-2855G= (SNHG31)
XM_011510951.1:c.7352+31C= (ABCA12)	XP_011509253.1:n.7352+31C=
XM_011510951.2:c.7352+31C= (ABCA12)	XP_011509253.1:n.7352+31C=
NM_173076.3:c.7343+31C= (ABCA12) MANE Select	NP_775099.2:n.7343+31C=
NR_103740.2:n.7841+31C= (ABCA12)
NM_015657.4:c.6389+31C= (ABCA12)	NP_056472.2:n.6389+31C=