Canonical Allele Identifier: CA379664963
Gene: CTR9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763778G>C , CM000673.2:g.10763778G>C GRCh38
NC_000011.9:g.10785325G>C , CM000673.1:g.10785325G>C GRCh37
NC_000011.8:g.10741901G>C NCBI36
NG_051671.1:g.17792G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1093G>C MANE Select ENSP00000355013.2:p.Glu365Gln
ENST00000361367.6:c.1093G>C ENSP00000355013.2:p.Glu365Gln
NM_014633.4:c.1093G>C NP_055448.1:p.Glu365Gln
NM_001346279.1:c.1093G>C NP_001333208.1:p.Glu365Gln
NM_014633.5:c.1093G>C MANE Select NP_055448.1:p.Glu365Gln
NM_001346279.2:c.1093G>C NP_001333208.1:p.Glu365Gln