Canonical Allele Identifier: CA1952042764

Gene: CTR9

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.10763746G= , CM000673.2:g.10763746G=	GRCh38
NC_000011.9:g.10785293G= , CM000673.1:g.10785293G=	GRCh37
NC_000011.8:g.10741869G=	NCBI36
NG_051671.1:g.17760G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361367.7:c.1061G= MANE Select	ENSP00000355013.2:p.Arg354=
ENST00000361367.6:c.1061G=	ENSP00000355013.2:p.Arg354=
NM_014633.4:c.1061G=	NP_055448.1:p.Arg354=
NM_001346279.1:c.1061G=	NP_001333208.1:p.Arg354=
NM_014633.5:c.1061G= MANE Select	NP_055448.1:p.Arg354=
NM_001346279.2:c.1061G=	NP_001333208.1:p.Arg354=