Canonical Allele Identifier: CA3706066

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922159C>T , CM000668.2:g.30922159C>T	GRCh38
NC_000006.11:g.30889936C>T , CM000668.1:g.30889936C>T	GRCh37
NC_000006.10:g.30997915C>T	NCBI36
NG_034224.1:g.12952C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020442.6:c.1850C>T MANE Select	NP_065175.4:p.Thr617Met
ENST00000676266.1:c.1850C>T MANE Select	ENSP00000502585.1:p.Thr617Met
NM_001167733.2:c.1430C>T	NP_001161205.1:p.Thr477Met
NM_001167733.3:c.1430C>T	NP_001161205.1:p.Thr477Met
NM_001167734.1:c.1940C>T	NP_001161206.1:p.Thr647Met
NM_001167734.2:c.1940C>T	NP_001161206.1:p.Thr647Met
NM_020442.5:c.1850C>T	NP_065175.4:p.Thr617Met
ENST00000321897.9:c.1850C>T	ENSP00000316092.5:p.Thr617Met
ENST00000469358.5:n.1770C>T
ENST00000476162.5:n.637C>T
ENST00000477288.5:n.4463C>T
ENST00000541562.5:c.1940C>T	ENSP00000441000.1:p.Thr647Met
ENST00000541562.6:c.1850C>T	ENSP00000441000.2:p.Thr617Met
ENST00000542001.5:c.1844C>T	ENSP00000438200.2:p.Thr615Met
ENST00000625423.2:c.1430C>T	ENSP00000485818.1:p.Thr477Met
ENST00000672801.1:c.1844C>T	ENSP00000500615.1:p.Thr615Met