Canonical Allele Identifier: CA1047787909
Gene: TRAIP HGNC NCBI

Linked Data

dbSNP Id: rs2081705047
gnomAD v3: 3-49828780-A-G
gnomAD v4: 3-49828780-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828780A>G , CM000665.2:g.49828780A>G GRCh38
NC_000003.11:g.49866213A>G , CM000665.1:g.49866213A>G GRCh37
NC_000003.10:g.49841217A>G NCBI36
NG_046695.1:g.32780T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*323T>C MANE Select ENSP00000328203.2:n.*323T>C
ENST00000331456.6:c.*323T>C ENSP00000328203.2:n.*323T>C
ENST00000491060.1:n.887T>C
NM_005879.2:c.*323T>C NP_005870.2:n.*323T>C
XM_011533264.1:c.*323T>C XP_011531566.1:n.*323T>C
XM_017005526.1:c.*323T>C XP_016861015.1:n.*323T>C
XR_001739979.1:n.1937T>C
NM_005879.3:c.*323T>C MANE Select NP_005870.2:n.*323T>C
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