Canonical Allele Identifier: CA449584324

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30921612T>G , CM000668.2:g.30921612T>G	GRCh38
NC_000006.11:g.30889389T>G , CM000668.1:g.30889389T>G	GRCh37
NC_000006.10:g.30997368T>G	NCBI36
NG_034224.1:g.12405T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.1656T>G	ENSP00000441000.2:p.Val552=
ENST00000672801.1:c.1650T>G	ENSP00000500615.1:p.Val550=
ENST00000676266.1:c.1656T>G MANE Select	ENSP00000502585.1:p.Val552=
ENST00000321897.9:c.1656T>G	ENSP00000316092.5:p.Val552=
ENST00000469358.5:n.1576T>G
ENST00000476162.5:n.514T>G
ENST00000477288.5:n.4269T>G
ENST00000541562.5:c.1746T>G	ENSP00000441000.1:p.Val582=
ENST00000542001.5:c.1650T>G	ENSP00000438200.2:p.Val550=
ENST00000625423.2:c.1236T>G	ENSP00000485818.1:p.Val412=
NM_001167733.2:c.1236T>G	NP_001161205.1:p.Val412=
NM_001167734.1:c.1746T>G	NP_001161206.1:p.Val582=
NM_020442.5:c.1656T>G	NP_065175.4:p.Val552=
NM_001167733.3:c.1236T>G	NP_001161205.1:p.Val412=
NM_001167734.2:c.1746T>G	NP_001161206.1:p.Val582=
NM_020442.6:c.1656T>G MANE Select	NP_065175.4:p.Val552=