Canonical Allele Identifier: CA379664614
Gene: CTR9 HGNC NCBI

Linked Data

gnomAD v4: 11-10763716-T-C
MyVariant Identifiers: chr11:g.10785263T>C (hg19) chr11:g.10763716T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763716T>C , CM000673.2:g.10763716T>C GRCh38
NC_000011.9:g.10785263T>C , CM000673.1:g.10785263T>C GRCh37
NC_000011.8:g.10741839T>C NCBI36
NG_051671.1:g.17730T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1031T>C MANE Select ENSP00000355013.2:p.Phe344Ser
ENST00000361367.6:c.1031T>C ENSP00000355013.2:p.Phe344Ser
ENST00000524523.1:c.884T>C ENSP00000431458.1:p.Phe295Ser
NM_014633.4:c.1031T>C NP_055448.1:p.Phe344Ser
NM_001346279.1:c.1031T>C NP_001333208.1:p.Phe344Ser
NM_014633.5:c.1031T>C MANE Select NP_055448.1:p.Phe344Ser
NM_001346279.2:c.1031T>C NP_001333208.1:p.Phe344Ser
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