Canonical Allele Identifier: CA566687351
Gene: VARS2 HGNC NCBI

Linked Data

dbSNP Id: rs1368265356

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30922980dup , CM000668.2:g.30922980dup GRCh38
NC_000006.11:g.30890757dup , CM000668.1:g.30890757dup GRCh37
NC_000006.10:g.30998736dup NCBI36
NG_034224.1:g.13773dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000541562.6:c.2185+4dup ENSP00000441000.2:n.2185+4dup
ENST00000672801.1:c.2179+4dup ENSP00000500615.1:n.2179+4dup
ENST00000676266.1:c.2185+4dup MANE Select ENSP00000502585.1:n.2185+4dup
ENST00000321897.9:c.2185+4dup ENSP00000316092.5:n.2185+4dup
ENST00000469358.5:n.2173+4dup
ENST00000476162.5:n.972+4dup
ENST00000477052.1:n.271+4dup
ENST00000477288.5:n.4798+4dup
ENST00000541562.5:c.2275+4dup ENSP00000441000.1:n.2275+4dup
ENST00000542001.5:c.2179+4dup ENSP00000438200.2:n.2179+4dup
ENST00000625423.2:c.1765+4dup ENSP00000485818.1:n.1765+4dup
NM_001167733.2:c.1765+4dup NP_001161205.1:n.1765+4dup
NM_001167734.1:c.2275+4dup NP_001161206.1:n.2275+4dup
NM_020442.5:c.2185+4dup NP_065175.4:n.2185+4dup
NM_001167733.3:c.1765+4dup NP_001161205.1:n.1765+4dup
NM_001167734.2:c.2275+4dup NP_001161206.1:n.2275+4dup
NM_020442.6:c.2185+4dup MANE Select NP_065175.4:n.2185+4dup