Canonical Allele Identifier: CA9793587
Gene: VSX1 HGNC NCBI

Linked Data

dbSNP Id: rs138766673

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.25078900C>A , CM000682.2:g.25078900C>A GRCh38
NC_000020.10:g.25059536C>A , CM000682.1:g.25059536C>A GRCh37
NC_000020.9:g.25007536C>A NCBI36
NG_008101.1:g.8232G>T
NG_008101.2:g.8232G>T
NG_008101.3:g.8282G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376709.9:c.556G>T MANE Select ENSP00000365899.3:p.Ala186Ser
ENST00000376707.4:c.556G>T ENSP00000365897.3:p.Ala186Ser
ENST00000376709.8:c.556G>T ENSP00000365899.3:p.Ala186Ser
ENST00000409285.6:c.556G>T ENSP00000386612.2:p.Ala186Ser
ENST00000409958.6:c.556G>T ENSP00000387069.2:p.Ala186Ser
ENST00000429762.7:c.556G>T ENSP00000401690.3:p.Ala186Ser
ENST00000444511.6:c.556G>T ENSP00000387720.2:p.Ala186Ser
NM_001256271.1:c.556G>T NP_001243200.1:p.Ala186Ser
NM_001256272.1:c.556G>T NP_001243201.1:p.Ala186Ser
NM_014588.5:c.556G>T NP_055403.2:p.Ala186Ser
NM_199425.2:c.556G>T NP_955457.1:p.Ala186Ser
NR_045948.1:n.839G>T
NR_045951.1:n.839G>T
XM_017027837.1:c.556G>T XP_016883326.1:p.Ala186Ser
XM_017027838.1:c.556G>T XP_016883327.1:p.Ala186Ser
NM_014588.6:c.556G>T MANE Select NP_055403.2:p.Ala186Ser
NR_165181.1:n.314G>T
NM_001256271.2:c.556G>T NP_001243200.1:p.Ala186Ser
NM_001256272.2:c.556G>T NP_001243201.1:p.Ala186Ser
NM_199425.3:c.556G>T NP_955457.1:p.Ala186Ser
NR_045948.2:n.601G>T
NR_045951.2:n.601G>T
NR_165181.2:n.196G>T