Canonical Allele Identifier: CA2652202563
Gene: VSX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.25081639_25081640del , CM000682.2:g.25081639_25081640del GRCh38
NC_000020.10:g.25062275_25062276del , CM000682.1:g.25062275_25062276del GRCh37
NC_000020.9:g.25010275_25010276del NCBI36
NG_008101.1:g.5493_5494del
NG_008101.2:g.5493_5494del
NG_008101.3:g.5543_5544del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376709.9:c.424+34_424+35del MANE Select ENSP00000365899.3:n.424+34_424+35del
ENST00000376707.4:c.424+34_424+35del ENSP00000365897.3:n.424+34_424+35del
ENST00000376709.8:c.424+34_424+35del ENSP00000365899.3:n.424+34_424+35del
ENST00000409285.6:c.424+34_424+35del ENSP00000386612.2:n.424+34_424+35del
ENST00000409958.6:c.424+34_424+35del ENSP00000387069.2:n.424+34_424+35del
ENST00000429762.7:c.424+34_424+35del ENSP00000401690.3:n.424+34_424+35del
ENST00000444511.6:c.424+34_424+35del ENSP00000387720.2:n.424+34_424+35del
NM_001256271.1:c.424+34_424+35del NP_001243200.1:n.424+34_424+35del
NM_001256272.1:c.424+34_424+35del NP_001243201.1:n.424+34_424+35del
NM_014588.5:c.424+34_424+35del NP_055403.2:n.424+34_424+35del
NM_199425.2:c.424+34_424+35del NP_955457.1:n.424+34_424+35del
NR_045948.1:n.707+34_707+35del
NR_045951.1:n.707+34_707+35del
XM_017027837.1:c.424+34_424+35del XP_016883326.1:n.424+34_424+35del
XM_017027838.1:c.424+34_424+35del XP_016883327.1:n.424+34_424+35del
NM_014588.6:c.424+34_424+35del MANE Select NP_055403.2:n.424+34_424+35del
NM_001256271.2:c.424+34_424+35del NP_001243200.1:n.424+34_424+35del
NM_001256272.2:c.424+34_424+35del NP_001243201.1:n.424+34_424+35del
NM_199425.3:c.424+34_424+35del NP_955457.1:n.424+34_424+35del
NR_045948.2:n.469+34_469+35del
NR_045951.2:n.469+34_469+35del