Canonical Allele Identifier: CA1618928383

Gene: VARS2

Linked Data

• dbSNP Id: rs1794623163

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922983_30922988del , CM000668.2:g.30922983_30922988del	GRCh38
NC_000006.11:g.30890760_30890765del , CM000668.1:g.30890760_30890765del	GRCh37
NC_000006.10:g.30998739_30998744del	NCBI36
NG_034224.1:g.13776_13781del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2185+7_2185+12del	ENSP00000441000.2:n.2185+7_2185+12del
ENST00000672801.1:c.2179+7_2179+12del	ENSP00000500615.1:n.2179+7_2179+12del
ENST00000676266.1:c.2185+7_2185+12del MANE Select	ENSP00000502585.1:n.2185+7_2185+12del
ENST00000321897.9:c.2185+7_2185+12del	ENSP00000316092.5:n.2185+7_2185+12del
ENST00000469358.5:n.2173+7_2173+12del
ENST00000476162.5:n.972+7_972+12del
ENST00000477052.1:n.271+7_271+12del
ENST00000477288.5:n.4798+7_4798+12del
ENST00000541562.5:c.2275+7_2275+12del	ENSP00000441000.1:n.2275+7_2275+12del
ENST00000542001.5:c.2179+7_2179+12del	ENSP00000438200.2:n.2179+7_2179+12del
ENST00000625423.2:c.1765+7_1765+12del	ENSP00000485818.1:n.1765+7_1765+12del
NM_001167733.2:c.1765+7_1765+12del	NP_001161205.1:n.1765+7_1765+12del
NM_001167734.1:c.2275+7_2275+12del	NP_001161206.1:n.2275+7_2275+12del
NM_020442.5:c.2185+7_2185+12del	NP_065175.4:n.2185+7_2185+12del
NM_001167733.3:c.1765+7_1765+12del	NP_001161205.1:n.1765+7_1765+12del
NM_001167734.2:c.2275+7_2275+12del	NP_001161206.1:n.2275+7_2275+12del
NM_020442.6:c.2185+7_2185+12del MANE Select	NP_065175.4:n.2185+7_2185+12del