Canonical Allele Identifier: CA1363671531
Gene: TRAIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828962C= , CM000665.2:g.49828962C= GRCh38
NC_000003.11:g.49866395C= , CM000665.1:g.49866395C= GRCh37
NC_000003.10:g.49841399C= NCBI36
NG_046695.1:g.32598G=

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*141G= MANE Select ENSP00000328203.2:n.*141G=
ENST00000331456.6:c.*141G= ENSP00000328203.2:n.*141G=
ENST00000491060.1:n.705G=
NM_005879.2:c.*141G= NP_005870.2:n.*141G=
XM_011533264.1:c.*141G= XP_011531566.1:n.*141G=
XM_017005526.1:c.*141G= XP_016861015.1:n.*141G=
XR_001739979.1:n.1755G=
NM_005879.3:c.*141G= MANE Select NP_005870.2:n.*141G=