Canonical Allele Identifier: CA2665773791
Gene: TRAIP HGNC NCBI

Linked Data

gnomAD v4: 3-49828988-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828990del , CM000665.2:g.49828990del GRCh38
NC_000003.11:g.49866423del , CM000665.1:g.49866423del GRCh37
NC_000003.10:g.49841427del NCBI36
NG_046695.1:g.32571del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331456.7:c.*114del MANE Select ENSP00000328203.2:n.*114del
ENST00000331456.6:c.*114del ENSP00000328203.2:n.*114del
ENST00000491060.1:n.678del
NM_005879.2:c.*114del NP_005870.2:n.*114del
XM_011533264.1:c.*114del XP_011531566.1:n.*114del
XM_017005526.1:c.*114del XP_016861015.1:n.*114del
XR_001739979.1:n.1728del
NM_005879.3:c.*114del MANE Select NP_005870.2:n.*114del
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