Canonical Allele Identifier: CA363175777

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30891253T>C (hg19) ; chr6:g.30923476T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923476T>C , CM000668.2:g.30923476T>C	GRCh38
NC_000006.11:g.30891253T>C , CM000668.1:g.30891253T>C	GRCh37
NC_000006.10:g.30999232T>C	NCBI36
NG_034224.1:g.14269T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2437T>C	ENSP00000441000.2:p.Trp813Arg
ENST00000672801.1:c.2431T>C	ENSP00000500615.1:p.Trp811Arg
ENST00000676266.1:c.2437T>C MANE Select	ENSP00000502585.1:p.Trp813Arg
ENST00000321897.9:c.2437T>C	ENSP00000316092.5:p.Trp813Arg
ENST00000469358.5:n.2425T>C
ENST00000473916.1:n.148T>C
ENST00000476162.5:n.1224T>C
ENST00000477052.1:n.523T>C
ENST00000477288.5:n.5050T>C
ENST00000541562.5:c.2527T>C	ENSP00000441000.1:p.Trp843Arg
ENST00000542001.5:c.2431T>C	ENSP00000438200.2:p.Trp811Arg
ENST00000625423.2:c.2017T>C	ENSP00000485818.1:p.Trp673Arg
NM_001167733.2:c.2017T>C	NP_001161205.1:p.Trp673Arg
NM_001167734.1:c.2527T>C	NP_001161206.1:p.Trp843Arg
NM_020442.5:c.2437T>C	NP_065175.4:p.Trp813Arg
NM_001167733.3:c.2017T>C	NP_001161205.1:p.Trp673Arg
NM_001167734.2:c.2527T>C	NP_001161206.1:p.Trp843Arg
NM_020442.6:c.2437T>C MANE Select	NP_065175.4:p.Trp813Arg