Canonical Allele Identifier: CA379664669

Gene: CTR9

Linked Data

• MyVariant Identifiers: chr11:g.10785273G>T (hg19) ; chr11:g.10763726G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.10763726G>T , CM000673.2:g.10763726G>T	GRCh38
NC_000011.9:g.10785273G>T , CM000673.1:g.10785273G>T	GRCh37
NC_000011.8:g.10741849G>T	NCBI36
NG_051671.1:g.17740G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361367.7:c.1041G>T MANE Select	ENSP00000355013.2:p.Leu347Phe
ENST00000361367.6:c.1041G>T	ENSP00000355013.2:p.Leu347Phe
ENST00000524523.1:c.894G>T	ENSP00000431458.1:p.Leu298Phe
NM_014633.4:c.1041G>T	NP_055448.1:p.Leu347Phe
NM_001346279.1:c.1041G>T	NP_001333208.1:p.Leu347Phe
NM_014633.5:c.1041G>T MANE Select	NP_055448.1:p.Leu347Phe
NM_001346279.2:c.1041G>T	NP_001333208.1:p.Leu347Phe