Canonical Allele Identifier: CA1952042761
Gene: CTR9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763739A= , CM000673.2:g.10763739A= GRCh38
NC_000011.9:g.10785286A= , CM000673.1:g.10785286A= GRCh37
NC_000011.8:g.10741862A= NCBI36
NG_051671.1:g.17753A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1054A= MANE Select ENSP00000355013.2:p.Ile352=
ENST00000361367.6:c.1054A= ENSP00000355013.2:p.Ile352=
NM_014633.4:c.1054A= NP_055448.1:p.Ile352=
NM_001346279.1:c.1054A= NP_001333208.1:p.Ile352=
NM_014633.5:c.1054A= MANE Select NP_055448.1:p.Ile352=
NM_001346279.2:c.1054A= NP_001333208.1:p.Ile352=