Canonical Allele Identifier: CA1047787906
Gene: TRAIP HGNC NCBI

Linked Data

dbSNP Id: rs2081704918
gnomAD v3: 3-49828762-A-C
gnomAD v4: 3-49828762-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828762A>C , CM000665.2:g.49828762A>C GRCh38
NC_000003.11:g.49866195A>C , CM000665.1:g.49866195A>C GRCh37
NC_000003.10:g.49841199A>C NCBI36
NG_046695.1:g.32798T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*341T>G MANE Select ENSP00000328203.2:n.*341T>G
ENST00000331456.6:c.*341T>G ENSP00000328203.2:n.*341T>G
ENST00000491060.1:n.905T>G
NM_005879.2:c.*341T>G NP_005870.2:n.*341T>G
XM_011533264.1:c.*341T>G XP_011531566.1:n.*341T>G
XM_017005526.1:c.*341T>G XP_016861015.1:n.*341T>G
XR_001739979.1:n.1955T>G
NM_005879.3:c.*341T>G MANE Select NP_005870.2:n.*341T>G
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