Canonical Allele Identifier: CA379665060
Gene: CTR9 HGNC NCBI

Linked Data

gnomAD v4: 11-10763794-C-T
MyVariant Identifiers: chr11:g.10785341C>T (hg19) chr11:g.10763794C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763794C>T , CM000673.2:g.10763794C>T GRCh38
NC_000011.9:g.10785341C>T , CM000673.1:g.10785341C>T GRCh37
NC_000011.8:g.10741917C>T NCBI36
NG_051671.1:g.17808C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1109C>T MANE Select ENSP00000355013.2:p.Ala370Val
ENST00000361367.6:c.1109C>T ENSP00000355013.2:p.Ala370Val
NM_014633.4:c.1109C>T NP_055448.1:p.Ala370Val
NM_001346279.1:c.1109C>T NP_001333208.1:p.Ala370Val
NM_014633.5:c.1109C>T MANE Select NP_055448.1:p.Ala370Val
NM_001346279.2:c.1109C>T NP_001333208.1:p.Ala370Val
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