Canonical Allele Identifier: CA935091735
Gene: CTR9 HGNC NCBI

Linked Data

gnomAD v3: 11-10763720-TGG-T
gnomAD v4: 11-10763720-TGG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763721_10763722del , CM000673.2:g.10763721_10763722del GRCh38
NC_000011.9:g.10785268_10785269del , CM000673.1:g.10785268_10785269del GRCh37
NC_000011.8:g.10741844_10741845del NCBI36
NG_051671.1:g.17735_17736del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1036_1037del MANE Select ENSP00000355013.2:p.Gly346PhefsTer10
ENST00000361367.6:c.1036_1037del ENSP00000355013.2:p.Gly346PhefsTer10
ENST00000524523.1:c.889_890del ENSP00000431458.1:p.Gly297PhefsTer?
NM_014633.4:c.1036_1037del NP_055448.1:p.Gly346PhefsTer10
NM_001346279.1:c.1036_1037del NP_001333208.1:p.Gly346PhefsTer10
NM_014633.5:c.1036_1037del MANE Select NP_055448.1:p.Gly346PhefsTer10
NM_001346279.2:c.1036_1037del NP_001333208.1:p.Gly346PhefsTer10
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