Canonical Allele Identifier: CA408435919
Gene: VSX1 HGNC NCBI

Linked Data

dbSNP Id: rs6050307

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.25081706G>A , CM000682.2:g.25081706G>A GRCh38
NC_000020.10:g.25062342G>A , CM000682.1:g.25062342G>A GRCh37
NC_000020.9:g.25010342G>A NCBI36
NG_008101.1:g.5426C>T
NG_008101.2:g.5426C>T
NG_008101.3:g.5476C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376709.9:c.391C>T MANE Select ENSP00000365899.3:p.Arg131Cys
ENST00000376707.4:c.391C>T ENSP00000365897.3:p.Arg131Cys
ENST00000376709.8:c.391C>T ENSP00000365899.3:p.Arg131Cys
ENST00000409285.6:c.391C>T ENSP00000386612.2:p.Arg131Cys
ENST00000409958.6:c.391C>T ENSP00000387069.2:p.Arg131Cys
ENST00000429762.7:c.391C>T ENSP00000401690.3:p.Arg131Cys
ENST00000444511.6:c.391C>T ENSP00000387720.2:p.Arg131Cys
NM_001256271.1:c.391C>T NP_001243200.1:p.Arg131Cys
NM_001256272.1:c.391C>T NP_001243201.1:p.Arg131Cys
NM_014588.5:c.391C>T NP_055403.2:p.Arg131Cys
NM_199425.2:c.391C>T NP_955457.1:p.Arg131Cys
NR_045948.1:n.674C>T
NR_045951.1:n.674C>T
XM_017027837.1:c.391C>T XP_016883326.1:p.Arg131Cys
XM_017027838.1:c.391C>T XP_016883327.1:p.Arg131Cys
NM_014588.6:c.391C>T MANE Select NP_055403.2:p.Arg131Cys
NM_001256271.2:c.391C>T NP_001243200.1:p.Arg131Cys
NM_001256272.2:c.391C>T NP_001243201.1:p.Arg131Cys
NM_199425.3:c.391C>T NP_955457.1:p.Arg131Cys
NR_045948.2:n.436C>T
NR_045951.2:n.436C>T