Canonical Allele Identifier: CA2665773768
Gene: TRAIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828970del , CM000665.2:g.49828970del GRCh38
NC_000003.11:g.49866403del , CM000665.1:g.49866403del GRCh37
NC_000003.10:g.49841407del NCBI36
NG_046695.1:g.32592del

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*135del MANE Select ENSP00000328203.2:n.*135del
ENST00000331456.6:c.*135del ENSP00000328203.2:n.*135del
ENST00000491060.1:n.699del
NM_005879.2:c.*135del NP_005870.2:n.*135del
XM_011533264.1:c.*135del XP_011531566.1:n.*135del
XM_017005526.1:c.*135del XP_016861015.1:n.*135del
XR_001739979.1:n.1749del
NM_005879.3:c.*135del MANE Select NP_005870.2:n.*135del