Canonical Allele Identifier: CA473256598
Gene: CTR9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.10785276A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763729A>C , CM000673.2:g.10763729A>C GRCh38
NC_000011.9:g.10785276A>C , CM000673.1:g.10785276A>C GRCh37
NC_000011.8:g.10741852A>C NCBI36
NG_051671.1:g.17743A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1044A>C MANE Select ENSP00000355013.2:p.Gly348=
ENST00000361367.6:c.1044A>C ENSP00000355013.2:p.Gly348=
ENST00000524523.1:c.897A>C ENSP00000431458.1:p.Gly299=
NM_014633.4:c.1044A>C NP_055448.1:p.Gly348=
NM_001346279.1:c.1044A>C NP_001333208.1:p.Gly348=
NM_014633.5:c.1044A>C MANE Select NP_055448.1:p.Gly348=
NM_001346279.2:c.1044A>C NP_001333208.1:p.Gly348=
Search 100 bp 5'
Search 100 bp 3'