Canonical Allele Identifier: CA2665773788
Gene: TRAIP HGNC NCBI

Linked Data

gnomAD v4: 3-49828986-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828986C>T , CM000665.2:g.49828986C>T GRCh38
NC_000003.11:g.49866419C>T , CM000665.1:g.49866419C>T GRCh37
NC_000003.10:g.49841423C>T NCBI36
NG_046695.1:g.32574G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*117G>A MANE Select ENSP00000328203.2:n.*117G>A
ENST00000331456.6:c.*117G>A ENSP00000328203.2:n.*117G>A
ENST00000491060.1:n.681G>A
NM_005879.2:c.*117G>A NP_005870.2:n.*117G>A
XM_011533264.1:c.*117G>A XP_011531566.1:n.*117G>A
XM_017005526.1:c.*117G>A XP_016861015.1:n.*117G>A
XR_001739979.1:n.1731G>A
NM_005879.3:c.*117G>A MANE Select NP_005870.2:n.*117G>A
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