Canonical Allele Identifier: CA2665773761
Gene: TRAIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828970_49828975del , CM000665.2:g.49828970_49828975del GRCh38
NC_000003.11:g.49866403_49866408del , CM000665.1:g.49866403_49866408del GRCh37
NC_000003.10:g.49841407_49841412del NCBI36
NG_046695.1:g.32591_32596del

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*134_*139del MANE Select ENSP00000328203.2:n.*134_*139del
ENST00000331456.6:c.*134_*139del ENSP00000328203.2:n.*134_*139del
ENST00000491060.1:n.698_703del
NM_005879.2:c.*134_*139del NP_005870.2:n.*134_*139del
XM_011533264.1:c.*134_*139del XP_011531566.1:n.*134_*139del
XM_017005526.1:c.*134_*139del XP_016861015.1:n.*134_*139del
XR_001739979.1:n.1748_1753del
NM_005879.3:c.*134_*139del MANE Select NP_005870.2:n.*134_*139del