Canonical Allele Identifier: CA2665773754
Gene: TRAIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828959_49828964del , CM000665.2:g.49828959_49828964del GRCh38
NC_000003.11:g.49866392_49866397del , CM000665.1:g.49866392_49866397del GRCh37
NC_000003.10:g.49841396_49841401del NCBI36
NG_046695.1:g.32596_32601del

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*139_*144del MANE Select ENSP00000328203.2:n.*139_*144del
ENST00000331456.6:c.*139_*144del ENSP00000328203.2:n.*139_*144del
ENST00000491060.1:n.703_708del
NM_005879.2:c.*139_*144del NP_005870.2:n.*139_*144del
XM_011533264.1:c.*139_*144del XP_011531566.1:n.*139_*144del
XM_017005526.1:c.*139_*144del XP_016861015.1:n.*139_*144del
XR_001739979.1:n.1753_1758del
NM_005879.3:c.*139_*144del MANE Select NP_005870.2:n.*139_*144del