Canonical Allele Identifier: CA2665773622
Gene: TRAIP HGNC NCBI

Linked Data

gnomAD v4: 3-49828886-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828886A>T , CM000665.2:g.49828886A>T GRCh38
NC_000003.11:g.49866319A>T , CM000665.1:g.49866319A>T GRCh37
NC_000003.10:g.49841323A>T NCBI36
NG_046695.1:g.32674T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*217T>A MANE Select ENSP00000328203.2:n.*217T>A
ENST00000331456.6:c.*217T>A ENSP00000328203.2:n.*217T>A
ENST00000491060.1:n.781T>A
NM_005879.2:c.*217T>A NP_005870.2:n.*217T>A
XM_011533264.1:c.*217T>A XP_011531566.1:n.*217T>A
XM_017005526.1:c.*217T>A XP_016861015.1:n.*217T>A
XR_001739979.1:n.1831T>A
NM_005879.3:c.*217T>A MANE Select NP_005870.2:n.*217T>A
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