Canonical Allele Identifier: CA10217026
Gene: C1QTNF6 HGNC NCBI

Linked Data

dbSNP Id: rs143232740

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37185425C>T , CM000684.2:g.37185425C>T GRCh38
NC_000022.10:g.37581465C>T , CM000684.1:g.37581465C>T GRCh37
NC_000022.9:g.35911411C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337843.7:c.82G>A MANE Select ENSP00000338812.2:p.Val28Ile
ENST00000337843.6:c.82G>A ENSP00000338812.2:p.Val28Ile
ENST00000397110.6:c.82G>A ENSP00000380299.2:p.Val28Ile
ENST00000434784.1:c.82G>A ENSP00000399243.1:p.Val28Ile
ENST00000470655.5:n.3572G>A
ENST00000493023.1:n.524G>A
NM_031910.3:c.82G>A NP_114116.3:p.Val28Ile
NM_182486.1:c.82G>A NP_872292.1:p.Val28Ile
XM_006724125.2:c.25G>A XP_006724188.1:p.Val9Ile
XM_011529857.1:c.25G>A XP_011528159.1:p.Val9Ile
NM_001365878.1:c.25G>A NP_001352807.1:p.Val9Ile
XM_011529857.2:c.25G>A XP_011528159.1:p.Val9Ile
XM_017028569.1:c.82G>A XP_016884058.1:p.Val28Ile
XM_024452150.1:c.82G>A XP_024307918.1:p.Val28Ile
XM_024452151.1:c.82G>A XP_024307919.1:p.Val28Ile
XM_024452152.1:c.82G>A XP_024307920.1:p.Val28Ile
XM_024452153.1:c.82G>A XP_024307921.1:p.Val28Ile
XM_024452154.1:c.82G>A XP_024307922.1:p.Val28Ile
XM_024452155.1:c.25G>A XP_024307923.1:p.Val9Ile
NM_031910.4:c.82G>A MANE Select NP_114116.3:p.Val28Ile
NM_182486.2:c.82G>A NP_872292.1:p.Val28Ile