Canonical Allele Identifier: CA2677909336

Gene: VARS2

Linked Data

• gnomAD v4: 6-30923014-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923015_30923016del , CM000668.2:g.30923015_30923016del	GRCh38
NC_000006.11:g.30890792_30890793del , CM000668.1:g.30890792_30890793del	GRCh37
NC_000006.10:g.30998771_30998772del	NCBI36
NG_034224.1:g.13808_13809del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2185+39_2185+40del	ENSP00000441000.2:n.2185+39_2185+40del
ENST00000672801.1:c.2179+39_2179+40del	ENSP00000500615.1:n.2179+39_2179+40del
ENST00000676266.1:c.2185+39_2185+40del MANE Select	ENSP00000502585.1:n.2185+39_2185+40del
ENST00000321897.9:c.2185+39_2185+40del	ENSP00000316092.5:n.2185+39_2185+40del
ENST00000469358.5:n.2173+39_2173+40del
ENST00000476162.5:n.972+39_972+40del
ENST00000477052.1:n.271+39_271+40del
ENST00000477288.5:n.4798+39_4798+40del
ENST00000541562.5:c.2275+39_2275+40del	ENSP00000441000.1:n.2275+39_2275+40del
ENST00000542001.5:c.2179+39_2179+40del	ENSP00000438200.2:n.2179+39_2179+40del
ENST00000625423.2:c.1765+39_1765+40del	ENSP00000485818.1:n.1765+39_1765+40del
NM_001167733.2:c.1765+39_1765+40del	NP_001161205.1:n.1765+39_1765+40del
NM_001167734.1:c.2275+39_2275+40del	NP_001161206.1:n.2275+39_2275+40del
NM_020442.5:c.2185+39_2185+40del	NP_065175.4:n.2185+39_2185+40del
NM_001167733.3:c.1765+39_1765+40del	NP_001161205.1:n.1765+39_1765+40del
NM_001167734.2:c.2275+39_2275+40del	NP_001161206.1:n.2275+39_2275+40del
NM_020442.6:c.2185+39_2185+40del MANE Select	NP_065175.4:n.2185+39_2185+40del