Canonical Allele Identifier: CA324445
Gene: C10orf2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 4627
dbSNP Id: rs80356540

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100990474A>G , CM000672.2:g.100990474A>G GRCh38
NC_000010.10:g.102750231A>G , CM000672.1:g.102750231A>G GRCh37
NC_000010.9:g.102740221A>G NCBI36
NG_011646.1:g.2042T>C
NG_012624.1:g.7939A>G

Transcript Alleles

HGVS Amino-acid change
NM_001163812.1:c.1523A>G VV NP_001157284.1:p.Tyr508Cys
NM_001163813.1:c.161A>G VV NP_001157285.1:p.Tyr54Cys
NM_001163814.1:c.161A>G VV NP_001157286.1:p.Tyr54Cys
NM_021830.4:c.1523A>G VV NP_068602.2:p.Tyr508Cys
XM_011539974.1:c.161A>G XP_011538276.1:p.Tyr54Cys
XM_011539975.1:c.161A>G XP_011538277.1:p.Tyr54Cys
XR_945788.1:n.2294A>G
XM_011539975.2:c.161A>G XP_011538277.1:p.Tyr54Cys
XM_017016437.1:c.161A>G XP_016871926.1:p.Tyr54Cys
XR_001747142.1:n.1697A>G
XR_001747144.1:n.1635A>G
XR_002956991.1:n.1635A>G
XR_945788.2:n.1635A>G
NM_021830.5:c.1523A>G VV MANE Preferred NP_068602.2:p.Tyr508Cys
ENST00000311916.6:c.1523A>G ENSP00000309595.2:p.Tyr508Cys
ENST00000370228.1:c.1523A>G ENSP00000359248.1:p.Tyr508Cys
ENST00000473656.5:n.344A>G
ENST00000476766.5:n.409A>G