Canonical Allele Identifier: CA363175394

Gene: VARS2

Linked Data

• gnomAD v4: 6-30923382-G-T
• MyVariant Identifiers: chr6:g.30891159G>T (hg19) ; chr6:g.30923382G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923382G>T , CM000668.2:g.30923382G>T	GRCh38
NC_000006.11:g.30891159G>T , CM000668.1:g.30891159G>T	GRCh37
NC_000006.10:g.30999138G>T	NCBI36
NG_034224.1:g.14175G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2343G>T	ENSP00000441000.2:p.Trp781Cys
ENST00000672801.1:c.2337G>T	ENSP00000500615.1:p.Trp779Cys
ENST00000676266.1:c.2343G>T MANE Select	ENSP00000502585.1:p.Trp781Cys
ENST00000321897.9:c.2343G>T	ENSP00000316092.5:p.Trp781Cys
ENST00000469358.5:n.2331G>T
ENST00000473916.1:n.54G>T
ENST00000476162.5:n.1130G>T
ENST00000477052.1:n.429G>T
ENST00000477288.5:n.4956G>T
ENST00000541562.5:c.2433G>T	ENSP00000441000.1:p.Trp811Cys
ENST00000542001.5:c.2337G>T	ENSP00000438200.2:p.Trp779Cys
ENST00000625423.2:c.1923G>T	ENSP00000485818.1:p.Trp641Cys
NM_001167733.2:c.1923G>T	NP_001161205.1:p.Trp641Cys
NM_001167734.1:c.2433G>T	NP_001161206.1:p.Trp811Cys
NM_020442.5:c.2343G>T	NP_065175.4:p.Trp781Cys
NM_001167733.3:c.1923G>T	NP_001161205.1:p.Trp641Cys
NM_001167734.2:c.2433G>T	NP_001161206.1:p.Trp811Cys
NM_020442.6:c.2343G>T MANE Select	NP_065175.4:p.Trp781Cys