Canonical Allele Identifier: CA363174888

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890687C>A (hg19) ; chr6:g.30922910C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922910C>A , CM000668.2:g.30922910C>A	GRCh38
NC_000006.11:g.30890687C>A , CM000668.1:g.30890687C>A	GRCh37
NC_000006.10:g.30998666C>A	NCBI36
NG_034224.1:g.13703C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2119C>A	ENSP00000441000.2:p.Pro707Thr
ENST00000672801.1:c.2113C>A	ENSP00000500615.1:p.Pro705Thr
ENST00000676266.1:c.2119C>A MANE Select	ENSP00000502585.1:p.Pro707Thr
ENST00000321897.9:c.2119C>A	ENSP00000316092.5:p.Pro707Thr
ENST00000469358.5:n.2107C>A
ENST00000476162.5:n.906C>A
ENST00000477052.1:n.205C>A
ENST00000477288.5:n.4732C>A
ENST00000541562.5:c.2209C>A	ENSP00000441000.1:p.Pro737Thr
ENST00000542001.5:c.2113C>A	ENSP00000438200.2:p.Pro705Thr
ENST00000625423.2:c.1699C>A	ENSP00000485818.1:p.Pro567Thr
NM_001167733.2:c.1699C>A	NP_001161205.1:p.Pro567Thr
NM_001167734.1:c.2209C>A	NP_001161206.1:p.Pro737Thr
NM_020442.5:c.2119C>A	NP_065175.4:p.Pro707Thr
NM_001167733.3:c.1699C>A	NP_001161205.1:p.Pro567Thr
NM_001167734.2:c.2209C>A	NP_001161206.1:p.Pro737Thr
NM_020442.6:c.2119C>A MANE Select	NP_065175.4:p.Pro707Thr