Canonical Allele Identifier: CA1363671453
Gene: TRAIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828762A= , CM000665.2:g.49828762A= GRCh38
NC_000003.11:g.49866195A= , CM000665.1:g.49866195A= GRCh37
NC_000003.10:g.49841199A= NCBI36
NG_046695.1:g.32798T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331456.7:c.*341T= MANE Select ENSP00000328203.2:n.*341T=
ENST00000331456.6:c.*341T= ENSP00000328203.2:n.*341T=
ENST00000491060.1:n.905T=
NM_005879.2:c.*341T= NP_005870.2:n.*341T=
XM_011533264.1:c.*341T= XP_011531566.1:n.*341T=
XM_017005526.1:c.*341T= XP_016861015.1:n.*341T=
XR_001739979.1:n.1955T=
NM_005879.3:c.*341T= MANE Select NP_005870.2:n.*341T=