Canonical Allele Identifier: CA379665018
Gene: CTR9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.10785335T>A (hg19) chr11:g.10763788T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763788T>A , CM000673.2:g.10763788T>A GRCh38
NC_000011.9:g.10785335T>A , CM000673.1:g.10785335T>A GRCh37
NC_000011.8:g.10741911T>A NCBI36
NG_051671.1:g.17802T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1103T>A MANE Select ENSP00000355013.2:p.Leu368Ter
ENST00000361367.6:c.1103T>A ENSP00000355013.2:p.Leu368Ter
NM_014633.4:c.1103T>A NP_055448.1:p.Leu368Ter
NM_001346279.1:c.1103T>A NP_001333208.1:p.Leu368Ter
NM_014633.5:c.1103T>A MANE Select NP_055448.1:p.Leu368Ter
NM_001346279.2:c.1103T>A NP_001333208.1:p.Leu368Ter
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