Canonical Allele Identifier: CA2665773529
Gene: TRAIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828788_49828827del , CM000665.2:g.49828788_49828827del GRCh38
NC_000003.11:g.49866221_49866260del , CM000665.1:g.49866221_49866260del GRCh37
NC_000003.10:g.49841225_49841264del NCBI36
NG_046695.1:g.32736_32775del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331456.7:c.*279_*318del MANE Select ENSP00000328203.2:n.*279_*318del
ENST00000331456.6:c.*279_*318del ENSP00000328203.2:n.*279_*318del
ENST00000491060.1:n.843_882del
NM_005879.2:c.*279_*318del NP_005870.2:n.*279_*318del
XM_011533264.1:c.*279_*318del XP_011531566.1:n.*279_*318del
XM_017005526.1:c.*279_*318del XP_016861015.1:n.*279_*318del
XR_001739979.1:n.1893_1932del
NM_005879.3:c.*279_*318del MANE Select NP_005870.2:n.*279_*318del