Canonical Allele Identifier: CA1618928357

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922909T= , CM000668.2:g.30922909T=	GRCh38
NC_000006.11:g.30890686T= , CM000668.1:g.30890686T=	GRCh37
NC_000006.10:g.30998665T=	NCBI36
NG_034224.1:g.13702T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2118T=	ENSP00000441000.2:p.Phe706=
ENST00000672801.1:c.2112T=	ENSP00000500615.1:p.Phe704=
ENST00000676266.1:c.2118T= MANE Select	ENSP00000502585.1:p.Phe706=
ENST00000321897.9:c.2118T=	ENSP00000316092.5:p.Phe706=
ENST00000469358.5:n.2106T=
ENST00000476162.5:n.905T=
ENST00000477052.1:n.204T=
ENST00000477288.5:n.4731T=
ENST00000541562.5:c.2208T=	ENSP00000441000.1:p.Phe736=
ENST00000542001.5:c.2112T=	ENSP00000438200.2:p.Phe704=
ENST00000625423.2:c.1698T=	ENSP00000485818.1:p.Phe566=
NM_001167733.2:c.1698T=	NP_001161205.1:p.Phe566=
NM_001167734.1:c.2208T=	NP_001161206.1:p.Phe736=
NM_020442.5:c.2118T=	NP_065175.4:p.Phe706=
NM_001167733.3:c.1698T=	NP_001161205.1:p.Phe566=
NM_001167734.2:c.2208T=	NP_001161206.1:p.Phe736=
NM_020442.6:c.2118T= MANE Select	NP_065175.4:p.Phe706=