Canonical Allele Identifier: CA647883649
Gene: TRAIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828959_49828960insT , CM000665.2:g.49828959_49828960insT GRCh38
NC_000003.11:g.49866392_49866393insT , CM000665.1:g.49866392_49866393insT GRCh37
NC_000003.10:g.49841396_49841397insT NCBI36
NG_046695.1:g.32600_32601insA

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*143_*144insA MANE Select ENSP00000328203.2:n.*143_*144insA
ENST00000331456.6:c.*143_*144insA ENSP00000328203.2:n.*143_*144insA
ENST00000491060.1:n.707_708insA
NM_005879.2:c.*143_*144insA NP_005870.2:n.*143_*144insA
XM_011533264.1:c.*143_*144insA XP_011531566.1:n.*143_*144insA
XM_017005526.1:c.*143_*144insA XP_016861015.1:n.*143_*144insA
XR_001739979.1:n.1757_1758insA
NM_005879.3:c.*143_*144insA MANE Select NP_005870.2:n.*143_*144insA