Canonical Allele Identifier: CA907871364
Gene: TRAIP HGNC NCBI

Linked Data

dbSNP Id: rs1189075369

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828973_49828979del , CM000665.2:g.49828973_49828979del GRCh38
NC_000003.11:g.49866406_49866412del , CM000665.1:g.49866406_49866412del GRCh37
NC_000003.10:g.49841410_49841416del NCBI36
NG_046695.1:g.32581_32587del

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*124_*130del MANE Select ENSP00000328203.2:n.*124_*130del
ENST00000331456.6:c.*124_*130del ENSP00000328203.2:n.*124_*130del
ENST00000491060.1:n.688_694del
NM_005879.2:c.*124_*130del NP_005870.2:n.*124_*130del
XM_011533264.1:c.*124_*130del XP_011531566.1:n.*124_*130del
XM_017005526.1:c.*124_*130del XP_016861015.1:n.*124_*130del
XR_001739979.1:n.1738_1744del
NM_005879.3:c.*124_*130del MANE Select NP_005870.2:n.*124_*130del