Canonical Allele Identifier: CA379664983

Gene: CTR9

Linked Data

• gnomAD v4: 11-10763781-A-G
• MyVariant Identifiers: chr11:g.10785328A>G (hg19) ; chr11:g.10763781A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.10763781A>G , CM000673.2:g.10763781A>G	GRCh38
NC_000011.9:g.10785328A>G , CM000673.1:g.10785328A>G	GRCh37
NC_000011.8:g.10741904A>G	NCBI36
NG_051671.1:g.17795A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361367.7:c.1096A>G MANE Select	ENSP00000355013.2:p.Lys366Glu
ENST00000361367.6:c.1096A>G	ENSP00000355013.2:p.Lys366Glu
NM_014633.4:c.1096A>G	NP_055448.1:p.Lys366Glu
NM_001346279.1:c.1096A>G	NP_001333208.1:p.Lys366Glu
NM_014633.5:c.1096A>G MANE Select	NP_055448.1:p.Lys366Glu
NM_001346279.2:c.1096A>G	NP_001333208.1:p.Lys366Glu