Canonical Allele Identifier: CA1618928507
Gene: VARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30923263G= , CM000668.2:g.30923263G= GRCh38
NC_000006.11:g.30891040G= , CM000668.1:g.30891040G= GRCh37
NC_000006.10:g.30999019G= NCBI36
NG_034224.1:g.14056G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000541562.6:c.2313+32G= ENSP00000441000.2:n.2313+32G=
ENST00000672801.1:c.2307+32G= ENSP00000500615.1:n.2307+32G=
ENST00000676266.1:c.2313+32G= MANE Select ENSP00000502585.1:n.2313+32G=
ENST00000321897.9:c.2313+32G= ENSP00000316092.5:n.2313+32G=
ENST00000469358.5:n.2301+32G=
ENST00000473916.1:n.24+32G=
ENST00000476162.5:n.1100+32G=
ENST00000477052.1:n.399+32G=
ENST00000477288.5:n.4926+32G=
ENST00000541562.5:c.2403+32G= ENSP00000441000.1:n.2403+32G=
ENST00000542001.5:c.2307+32G= ENSP00000438200.2:n.2307+32G=
ENST00000625423.2:c.1893+32G= ENSP00000485818.1:n.1893+32G=
NM_001167733.2:c.1893+32G= NP_001161205.1:n.1893+32G=
NM_001167734.1:c.2403+32G= NP_001161206.1:n.2403+32G=
NM_020442.5:c.2313+32G= NP_065175.4:n.2313+32G=
NM_001167733.3:c.1893+32G= NP_001161205.1:n.1893+32G=
NM_001167734.2:c.2403+32G= NP_001161206.1:n.2403+32G=
NM_020442.6:c.2313+32G= MANE Select NP_065175.4:n.2313+32G=