Canonical Allele Identifier: CA2665773627
Gene: TRAIP HGNC NCBI

Linked Data

gnomAD v4: 3-49828889-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828889G>T , CM000665.2:g.49828889G>T GRCh38
NC_000003.11:g.49866322G>T , CM000665.1:g.49866322G>T GRCh37
NC_000003.10:g.49841326G>T NCBI36
NG_046695.1:g.32671C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*214C>A MANE Select ENSP00000328203.2:n.*214C>A
ENST00000331456.6:c.*214C>A ENSP00000328203.2:n.*214C>A
ENST00000491060.1:n.778C>A
NM_005879.2:c.*214C>A NP_005870.2:n.*214C>A
XM_011533264.1:c.*214C>A XP_011531566.1:n.*214C>A
XM_017005526.1:c.*214C>A XP_016861015.1:n.*214C>A
XR_001739979.1:n.1828C>A
NM_005879.3:c.*214C>A MANE Select NP_005870.2:n.*214C>A
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