Canonical Allele Identifier: CA2736711729
Gene: VSX1 HGNC NCBI

Linked Data

dbSNP Id: rs2122886469

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.25079095_25079096dup , CM000682.2:g.25079095_25079096dup GRCh38
NC_000020.10:g.25059731_25059732dup , CM000682.1:g.25059731_25059732dup GRCh37
NC_000020.9:g.25007731_25007732dup NCBI36
NG_008101.1:g.8036_8037dup
NG_008101.2:g.8036_8037dup
NG_008101.3:g.8086_8087dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376709.9:c.504-144_504-143dup MANE Select ENSP00000365899.3:n.504-144_504-143dup
ENST00000376707.4:c.504-144_504-143dup ENSP00000365897.3:n.504-144_504-143dup
ENST00000376709.8:c.504-144_504-143dup ENSP00000365899.3:n.504-144_504-143dup
ENST00000409285.6:c.504-144_504-143dup ENSP00000386612.2:n.504-144_504-143dup
ENST00000409958.6:c.504-144_504-143dup ENSP00000387069.2:n.504-144_504-143dup
ENST00000429762.7:c.504-144_504-143dup ENSP00000401690.3:n.504-144_504-143dup
ENST00000444511.6:c.504-144_504-143dup ENSP00000387720.2:n.504-144_504-143dup
NM_001256271.1:c.504-144_504-143dup NP_001243200.1:n.504-144_504-143dup
NM_001256272.1:c.504-144_504-143dup NP_001243201.1:n.504-144_504-143dup
NM_014588.5:c.504-144_504-143dup NP_055403.2:n.504-144_504-143dup
NM_199425.2:c.504-144_504-143dup NP_955457.1:n.504-144_504-143dup
NR_045948.1:n.787-144_787-143dup
NR_045951.1:n.787-144_787-143dup
XM_017027837.1:c.504-144_504-143dup XP_016883326.1:n.504-144_504-143dup
XM_017027838.1:c.504-144_504-143dup XP_016883327.1:n.504-144_504-143dup
NM_014588.6:c.504-144_504-143dup MANE Select NP_055403.2:n.504-144_504-143dup
NR_165181.1:n.262-144_262-143dup
NM_001256271.2:c.504-144_504-143dup NP_001243200.1:n.504-144_504-143dup
NM_001256272.2:c.504-144_504-143dup NP_001243201.1:n.504-144_504-143dup
NM_199425.3:c.504-144_504-143dup NP_955457.1:n.504-144_504-143dup
NR_045948.2:n.549-144_549-143dup
NR_045951.2:n.549-144_549-143dup
NR_165181.2:n.144-144_144-143dup