Canonical Allele Identifier: CA379664837
Gene: CTR9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763756A>T , CM000673.2:g.10763756A>T GRCh38
NC_000011.9:g.10785303A>T , CM000673.1:g.10785303A>T GRCh37
NC_000011.8:g.10741879A>T NCBI36
NG_051671.1:g.17770A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1071A>T MANE Select ENSP00000355013.2:p.Lys357Asn
ENST00000361367.6:c.1071A>T ENSP00000355013.2:p.Lys357Asn
NM_014633.4:c.1071A>T NP_055448.1:p.Lys357Asn
NM_001346279.1:c.1071A>T NP_001333208.1:p.Lys357Asn
NM_014633.5:c.1071A>T MANE Select NP_055448.1:p.Lys357Asn
NM_001346279.2:c.1071A>T NP_001333208.1:p.Lys357Asn