Canonical Allele Identifier: CA74578491
Gene: TRAIP HGNC NCBI

Linked Data

dbSNP Id: rs954615526

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828973dup , CM000665.2:g.49828973dup GRCh38
NC_000003.11:g.49866406dup , CM000665.1:g.49866406dup GRCh37
NC_000003.10:g.49841410dup NCBI36
NG_046695.1:g.32587dup

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*130dup MANE Select ENSP00000328203.2:n.*130dup
ENST00000331456.6:c.*130dup ENSP00000328203.2:n.*130dup
ENST00000491060.1:n.694dup
NM_005879.2:c.*130dup NP_005870.2:n.*130dup
XM_011533264.1:c.*130dup XP_011531566.1:n.*130dup
XM_017005526.1:c.*130dup XP_016861015.1:n.*130dup
XR_001739979.1:n.1744dup
NM_005879.3:c.*130dup MANE Select NP_005870.2:n.*130dup