Canonical Allele Identifier: CA363174961

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890721T>G (hg19) ; chr6:g.30922944T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922944T>G , CM000668.2:g.30922944T>G	GRCh38
NC_000006.11:g.30890721T>G , CM000668.1:g.30890721T>G	GRCh37
NC_000006.10:g.30998700T>G	NCBI36
NG_034224.1:g.13737T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2153T>G	ENSP00000441000.2:p.Leu718Arg
ENST00000672801.1:c.2147T>G	ENSP00000500615.1:p.Leu716Arg
ENST00000676266.1:c.2153T>G MANE Select	ENSP00000502585.1:p.Leu718Arg
ENST00000321897.9:c.2153T>G	ENSP00000316092.5:p.Leu718Arg
ENST00000469358.5:n.2141T>G
ENST00000476162.5:n.940T>G
ENST00000477052.1:n.239T>G
ENST00000477288.5:n.4766T>G
ENST00000541562.5:c.2243T>G	ENSP00000441000.1:p.Leu748Arg
ENST00000542001.5:c.2147T>G	ENSP00000438200.2:p.Leu716Arg
ENST00000625423.2:c.1733T>G	ENSP00000485818.1:p.Leu578Arg
NM_001167733.2:c.1733T>G	NP_001161205.1:p.Leu578Arg
NM_001167734.1:c.2243T>G	NP_001161206.1:p.Leu748Arg
NM_020442.5:c.2153T>G	NP_065175.4:p.Leu718Arg
NM_001167733.3:c.1733T>G	NP_001161205.1:p.Leu578Arg
NM_001167734.2:c.2243T>G	NP_001161206.1:p.Leu748Arg
NM_020442.6:c.2153T>G MANE Select	NP_065175.4:p.Leu718Arg