Canonical Allele Identifier: CA379665069
Gene: CTR9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763797A>G , CM000673.2:g.10763797A>G GRCh38
NC_000011.9:g.10785344A>G , CM000673.1:g.10785344A>G GRCh37
NC_000011.8:g.10741920A>G NCBI36
NG_051671.1:g.17811A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1112A>G MANE Select ENSP00000355013.2:p.Tyr371Cys
ENST00000361367.6:c.1112A>G ENSP00000355013.2:p.Tyr371Cys
NM_014633.4:c.1112A>G NP_055448.1:p.Tyr371Cys
NM_001346279.1:c.1112A>G NP_001333208.1:p.Tyr371Cys
NM_014633.5:c.1112A>G MANE Select NP_055448.1:p.Tyr371Cys
NM_001346279.2:c.1112A>G NP_001333208.1:p.Tyr371Cys