Canonical Allele Identifier: CA1363671548
Gene: TRAIP HGNC NCBI

Linked Data

dbSNP Id: rs2081707172
gnomAD v4: 3-49828989-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828989T>G , CM000665.2:g.49828989T>G GRCh38
NC_000003.11:g.49866422T>G , CM000665.1:g.49866422T>G GRCh37
NC_000003.10:g.49841426T>G NCBI36
NG_046695.1:g.32571A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331456.7:c.*114A>C MANE Select ENSP00000328203.2:n.*114A>C
ENST00000331456.6:c.*114A>C ENSP00000328203.2:n.*114A>C
ENST00000491060.1:n.678A>C
NM_005879.2:c.*114A>C NP_005870.2:n.*114A>C
XM_011533264.1:c.*114A>C XP_011531566.1:n.*114A>C
XM_017005526.1:c.*114A>C XP_016861015.1:n.*114A>C
XR_001739979.1:n.1728A>C
NM_005879.3:c.*114A>C MANE Select NP_005870.2:n.*114A>C
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