Canonical Allele Identifier: CA2665773521
Gene: TRAIP HGNC NCBI

Linked Data

gnomAD v4: 3-49828774-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828774A>C , CM000665.2:g.49828774A>C GRCh38
NC_000003.11:g.49866207A>C , CM000665.1:g.49866207A>C GRCh37
NC_000003.10:g.49841211A>C NCBI36
NG_046695.1:g.32786T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331456.7:c.*329T>G MANE Select ENSP00000328203.2:n.*329T>G
ENST00000331456.6:c.*329T>G ENSP00000328203.2:n.*329T>G
ENST00000491060.1:n.893T>G
NM_005879.2:c.*329T>G NP_005870.2:n.*329T>G
XM_011533264.1:c.*329T>G XP_011531566.1:n.*329T>G
XM_017005526.1:c.*329T>G XP_016861015.1:n.*329T>G
XR_001739979.1:n.1943T>G
NM_005879.3:c.*329T>G MANE Select NP_005870.2:n.*329T>G