Canonical Allele Identifier: CA1618928332

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922847_30922848delinsGC , CM000668.2:g.30922847_30922848delinsGC	GRCh38
NC_000006.11:g.30890624_30890625delinsGC , CM000668.1:g.30890624_30890625delinsGC	GRCh37
NC_000006.10:g.30998603_30998604delinsGC	NCBI36
NG_034224.1:g.13640_13641delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2107-51_2107-50delinsGC	ENSP00000441000.2:n.2107-51_2107-50delinsGC
ENST00000672801.1:c.2101-51_2101-50delinsGC	ENSP00000500615.1:n.2101-51_2101-50delinsGC
ENST00000676266.1:c.2107-51_2107-50delinsGC MANE Select	ENSP00000502585.1:n.2107-51_2107-50delinsGC
ENST00000321897.9:c.2107-51_2107-50delinsGC	ENSP00000316092.5:n.2107-51_2107-50delinsGC
ENST00000469358.5:n.2095-51_2095-50delinsGC
ENST00000476162.5:n.894-51_894-50delinsGC
ENST00000477052.1:n.193-51_193-50delinsGC
ENST00000477288.5:n.4720-51_4720-50delinsGC
ENST00000541562.5:c.2197-51_2197-50delinsGC	ENSP00000441000.1:n.2197-51_2197-50delinsGC
ENST00000542001.5:c.2101-51_2101-50delinsGC	ENSP00000438200.2:n.2101-51_2101-50delinsGC
ENST00000625423.2:c.1687-51_1687-50delinsGC	ENSP00000485818.1:n.1687-51_1687-50delinsGC
NM_001167733.2:c.1687-51_1687-50delinsGC	NP_001161205.1:n.1687-51_1687-50delinsGC
NM_001167734.1:c.2197-51_2197-50delinsGC	NP_001161206.1:n.2197-51_2197-50delinsGC
NM_020442.5:c.2107-51_2107-50delinsGC	NP_065175.4:n.2107-51_2107-50delinsGC
NM_001167733.3:c.1687-51_1687-50delinsGC	NP_001161205.1:n.1687-51_1687-50delinsGC
NM_001167734.2:c.2197-51_2197-50delinsGC	NP_001161206.1:n.2197-51_2197-50delinsGC
NM_020442.6:c.2107-51_2107-50delinsGC MANE Select	NP_065175.4:n.2107-51_2107-50delinsGC