Canonical Allele Identifier: CA379665091
Gene: CTR9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763800C>T , CM000673.2:g.10763800C>T GRCh38
NC_000011.9:g.10785347C>T , CM000673.1:g.10785347C>T GRCh37
NC_000011.8:g.10741923C>T NCBI36
NG_051671.1:g.17814C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1115C>T MANE Select ENSP00000355013.2:p.Pro372Leu
ENST00000361367.6:c.1115C>T ENSP00000355013.2:p.Pro372Leu
NM_014633.4:c.1115C>T NP_055448.1:p.Pro372Leu
NM_001346279.1:c.1115C>T NP_001333208.1:p.Pro372Leu
NM_014633.5:c.1115C>T MANE Select NP_055448.1:p.Pro372Leu
NM_001346279.2:c.1115C>T NP_001333208.1:p.Pro372Leu