Canonical Allele Identifier: CA1618928344

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922875_30922878delinsCCTT , CM000668.2:g.30922875_30922878delinsCCTT	GRCh38
NC_000006.11:g.30890652_30890655delinsCCTT , CM000668.1:g.30890652_30890655delinsCCTT	GRCh37
NC_000006.10:g.30998631_30998634delinsCCTT	NCBI36
NG_034224.1:g.13668_13671delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2107-23_2107-20delinsCCTT	ENSP00000441000.2:n.2107-23_2107-20delinsCCTT
ENST00000672801.1:c.2101-23_2101-20delinsCCTT	ENSP00000500615.1:n.2101-23_2101-20delinsCCTT
ENST00000676266.1:c.2107-23_2107-20delinsCCTT MANE Select	ENSP00000502585.1:n.2107-23_2107-20delinsCCTT
ENST00000321897.9:c.2107-23_2107-20delinsCCTT	ENSP00000316092.5:n.2107-23_2107-20delinsCCTT
ENST00000469358.5:n.2095-23_2095-20delinsCCTT
ENST00000476162.5:n.894-23_894-20delinsCCTT
ENST00000477052.1:n.193-23_193-20delinsCCTT
ENST00000477288.5:n.4720-23_4720-20delinsCCTT
ENST00000541562.5:c.2197-23_2197-20delinsCCTT	ENSP00000441000.1:n.2197-23_2197-20delinsCCTT
ENST00000542001.5:c.2101-23_2101-20delinsCCTT	ENSP00000438200.2:n.2101-23_2101-20delinsCCTT
ENST00000625423.2:c.1687-23_1687-20delinsCCTT	ENSP00000485818.1:n.1687-23_1687-20delinsCCTT
NM_001167733.2:c.1687-23_1687-20delinsCCTT	NP_001161205.1:n.1687-23_1687-20delinsCCTT
NM_001167734.1:c.2197-23_2197-20delinsCCTT	NP_001161206.1:n.2197-23_2197-20delinsCCTT
NM_020442.5:c.2107-23_2107-20delinsCCTT	NP_065175.4:n.2107-23_2107-20delinsCCTT
NM_001167733.3:c.1687-23_1687-20delinsCCTT	NP_001161205.1:n.1687-23_1687-20delinsCCTT
NM_001167734.2:c.2197-23_2197-20delinsCCTT	NP_001161206.1:n.2197-23_2197-20delinsCCTT
NM_020442.6:c.2107-23_2107-20delinsCCTT MANE Select	NP_065175.4:n.2107-23_2107-20delinsCCTT