Canonical Allele Identifier: CA2356696347
Gene: VSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.25078720A= , CM000682.2:g.25078720A= GRCh38
NC_000020.10:g.25059356A= , CM000682.1:g.25059356A= GRCh37
NC_000020.9:g.25007356A= NCBI36
NG_008101.1:g.8412T=
NG_008101.2:g.8412T=
NG_008101.3:g.8462T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376709.9:c.627+109T= MANE Select ENSP00000365899.3:n.627+109T=
ENST00000376707.4:c.*16T= ENSP00000365897.3:n.*16T=
ENST00000376709.8:c.627+109T= ENSP00000365899.3:n.627+109T=
ENST00000409285.6:c.627+109T= ENSP00000386612.2:n.627+109T=
ENST00000409958.6:c.627+109T= ENSP00000387069.2:n.627+109T=
ENST00000429762.7:c.627+109T= ENSP00000401690.3:n.627+109T=
ENST00000444511.6:c.627+109T= ENSP00000387720.2:n.627+109T=
NM_001256271.1:c.627+109T= NP_001243200.1:n.627+109T=
NM_001256272.1:c.627+109T= NP_001243201.1:n.627+109T=
NM_014588.5:c.627+109T= NP_055403.2:n.627+109T=
NM_199425.2:c.*16T= NP_955457.1:n.*16T=
NR_045948.1:n.910+109T=
NR_045951.1:n.910+109T=
XM_017027837.1:c.627+109T= XP_016883326.1:n.627+109T=
XM_017027838.1:c.627+109T= XP_016883327.1:n.627+109T=
NM_014588.6:c.627+109T= MANE Select NP_055403.2:n.627+109T=
NR_165181.1:n.385+109T=
NM_001256271.2:c.627+109T= NP_001243200.1:n.627+109T=
NM_001256272.2:c.627+109T= NP_001243201.1:n.627+109T=
NM_199425.3:c.*16T= NP_955457.1:n.*16T=
NR_045948.2:n.672+109T=
NR_045951.2:n.672+109T=
NR_165181.2:n.267+109T=