Canonical Allele Identifier: CA1618928356

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922905A= , CM000668.2:g.30922905A=	GRCh38
NC_000006.11:g.30890682A= , CM000668.1:g.30890682A=	GRCh37
NC_000006.10:g.30998661A=	NCBI36
NG_034224.1:g.13698A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2114A=	ENSP00000441000.2:p.Asp705=
ENST00000672801.1:c.2108A=	ENSP00000500615.1:p.Asp703=
ENST00000676266.1:c.2114A= MANE Select	ENSP00000502585.1:p.Asp705=
ENST00000321897.9:c.2114A=	ENSP00000316092.5:p.Asp705=
ENST00000469358.5:n.2102A=
ENST00000476162.5:n.901A=
ENST00000477052.1:n.200A=
ENST00000477288.5:n.4727A=
ENST00000541562.5:c.2204A=	ENSP00000441000.1:p.Asp735=
ENST00000542001.5:c.2108A=	ENSP00000438200.2:p.Asp703=
ENST00000625423.2:c.1694A=	ENSP00000485818.1:p.Asp565=
NM_001167733.2:c.1694A=	NP_001161205.1:p.Asp565=
NM_001167734.1:c.2204A=	NP_001161206.1:p.Asp735=
NM_020442.5:c.2114A=	NP_065175.4:p.Asp705=
NM_001167733.3:c.1694A=	NP_001161205.1:p.Asp565=
NM_001167734.2:c.2204A=	NP_001161206.1:p.Asp735=
NM_020442.6:c.2114A= MANE Select	NP_065175.4:p.Asp705=