Canonical Allele Identifier: CA408435371
Gene: VSX1 HGNC NCBI

Linked Data

dbSNP Id: rs2089574676

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.25078913C>G , CM000682.2:g.25078913C>G GRCh38
NC_000020.10:g.25059549C>G , CM000682.1:g.25059549C>G GRCh37
NC_000020.9:g.25007549C>G NCBI36
NG_008101.1:g.8219G>C
NG_008101.2:g.8219G>C
NG_008101.3:g.8269G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376709.9:c.543G>C MANE Select ENSP00000365899.3:p.Lys181Asn
ENST00000376707.4:c.543G>C ENSP00000365897.3:p.Lys181Asn
ENST00000376709.8:c.543G>C ENSP00000365899.3:p.Lys181Asn
ENST00000409285.6:c.543G>C ENSP00000386612.2:p.Lys181Asn
ENST00000409958.6:c.543G>C ENSP00000387069.2:p.Lys181Asn
ENST00000429762.7:c.543G>C ENSP00000401690.3:p.Lys181Asn
ENST00000444511.6:c.543G>C ENSP00000387720.2:p.Lys181Asn
NM_001256271.1:c.543G>C NP_001243200.1:p.Lys181Asn
NM_001256272.1:c.543G>C NP_001243201.1:p.Lys181Asn
NM_014588.5:c.543G>C NP_055403.2:p.Lys181Asn
NM_199425.2:c.543G>C NP_955457.1:p.Lys181Asn
NR_045948.1:n.826G>C
NR_045951.1:n.826G>C
XM_017027837.1:c.543G>C XP_016883326.1:p.Lys181Asn
XM_017027838.1:c.543G>C XP_016883327.1:p.Lys181Asn
NM_014588.6:c.543G>C MANE Select NP_055403.2:p.Lys181Asn
NR_165181.1:n.301G>C
NM_001256271.2:c.543G>C NP_001243200.1:p.Lys181Asn
NM_001256272.2:c.543G>C NP_001243201.1:p.Lys181Asn
NM_199425.3:c.543G>C NP_955457.1:p.Lys181Asn
NR_045948.2:n.588G>C
NR_045951.2:n.588G>C
NR_165181.2:n.183G>C