Canonical Allele Identifier: CA363175525

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30891198G>C (hg19) ; chr6:g.30923421G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923421G>C , CM000668.2:g.30923421G>C	GRCh38
NC_000006.11:g.30891198G>C , CM000668.1:g.30891198G>C	GRCh37
NC_000006.10:g.30999177G>C	NCBI36
NG_034224.1:g.14214G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2382G>C	ENSP00000441000.2:p.Glu794Asp
ENST00000672801.1:c.2376G>C	ENSP00000500615.1:p.Glu792Asp
ENST00000676266.1:c.2382G>C MANE Select	ENSP00000502585.1:p.Glu794Asp
ENST00000321897.9:c.2382G>C	ENSP00000316092.5:p.Glu794Asp
ENST00000469358.5:n.2370G>C
ENST00000473916.1:n.93G>C
ENST00000476162.5:n.1169G>C
ENST00000477052.1:n.468G>C
ENST00000477288.5:n.4995G>C
ENST00000541562.5:c.2472G>C	ENSP00000441000.1:p.Glu824Asp
ENST00000542001.5:c.2376G>C	ENSP00000438200.2:p.Glu792Asp
ENST00000625423.2:c.1962G>C	ENSP00000485818.1:p.Glu654Asp
NM_001167733.2:c.1962G>C	NP_001161205.1:p.Glu654Asp
NM_001167734.1:c.2472G>C	NP_001161206.1:p.Glu824Asp
NM_020442.5:c.2382G>C	NP_065175.4:p.Glu794Asp
NM_001167733.3:c.1962G>C	NP_001161205.1:p.Glu654Asp
NM_001167734.2:c.2472G>C	NP_001161206.1:p.Glu824Asp
NM_020442.6:c.2382G>C MANE Select	NP_065175.4:p.Glu794Asp