Canonical Allele Identifier: CA2702742148
Gene: TRAIP HGNC NCBI

Linked Data

dbSNP Id: rs2108307620
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828777_49828778del , CM000665.2:g.49828777_49828778del GRCh38
NC_000003.11:g.49866210_49866211del , CM000665.1:g.49866210_49866211del GRCh37
NC_000003.10:g.49841214_49841215del NCBI36
NG_046695.1:g.32785_32786del

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*328_*329del MANE Select ENSP00000328203.2:n.*328_*329del
ENST00000331456.6:c.*328_*329del ENSP00000328203.2:n.*328_*329del
ENST00000491060.1:n.892_893del
NM_005879.2:c.*328_*329del NP_005870.2:n.*328_*329del
XM_011533264.1:c.*328_*329del XP_011531566.1:n.*328_*329del
XM_017005526.1:c.*328_*329del XP_016861015.1:n.*328_*329del
XR_001739979.1:n.1942_1943del
NM_005879.3:c.*328_*329del MANE Select NP_005870.2:n.*328_*329del
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