Canonical Allele Identifier: CA1618928363

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922920T= , CM000668.2:g.30922920T=	GRCh38
NC_000006.11:g.30890697T= , CM000668.1:g.30890697T=	GRCh37
NC_000006.10:g.30998676T=	NCBI36
NG_034224.1:g.13713T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2129T=	ENSP00000441000.2:p.Ile710=
ENST00000672801.1:c.2123T=	ENSP00000500615.1:p.Ile708=
ENST00000676266.1:c.2129T= MANE Select	ENSP00000502585.1:p.Ile710=
ENST00000321897.9:c.2129T=	ENSP00000316092.5:p.Ile710=
ENST00000469358.5:n.2117T=
ENST00000476162.5:n.916T=
ENST00000477052.1:n.215T=
ENST00000477288.5:n.4742T=
ENST00000541562.5:c.2219T=	ENSP00000441000.1:p.Ile740=
ENST00000542001.5:c.2123T=	ENSP00000438200.2:p.Ile708=
ENST00000625423.2:c.1709T=	ENSP00000485818.1:p.Ile570=
NM_001167733.2:c.1709T=	NP_001161205.1:p.Ile570=
NM_001167734.1:c.2219T=	NP_001161206.1:p.Ile740=
NM_020442.5:c.2129T=	NP_065175.4:p.Ile710=
NM_001167733.3:c.1709T=	NP_001161205.1:p.Ile570=
NM_001167734.2:c.2219T=	NP_001161206.1:p.Ile740=
NM_020442.6:c.2129T= MANE Select	NP_065175.4:p.Ile710=