Canonical Allele Identifier: CA2665773517
Gene: TRAIP HGNC NCBI

Linked Data

gnomAD v4: 3-49828766-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828766T>G , CM000665.2:g.49828766T>G GRCh38
NC_000003.11:g.49866199T>G , CM000665.1:g.49866199T>G GRCh37
NC_000003.10:g.49841203T>G NCBI36
NG_046695.1:g.32794A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331456.7:c.*337A>C MANE Select ENSP00000328203.2:n.*337A>C
ENST00000331456.6:c.*337A>C ENSP00000328203.2:n.*337A>C
ENST00000491060.1:n.901A>C
NM_005879.2:c.*337A>C NP_005870.2:n.*337A>C
XM_011533264.1:c.*337A>C XP_011531566.1:n.*337A>C
XM_017005526.1:c.*337A>C XP_016861015.1:n.*337A>C
XR_001739979.1:n.1951A>C
NM_005879.3:c.*337A>C MANE Select NP_005870.2:n.*337A>C
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