Canonical Allele Identifier: CA2665773603
Gene: TRAIP HGNC NCBI

Linked Data

gnomAD v4: 3-49828869-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828869G>C , CM000665.2:g.49828869G>C GRCh38
NC_000003.11:g.49866302G>C , CM000665.1:g.49866302G>C GRCh37
NC_000003.10:g.49841306G>C NCBI36
NG_046695.1:g.32691C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*234C>G MANE Select ENSP00000328203.2:n.*234C>G
ENST00000331456.6:c.*234C>G ENSP00000328203.2:n.*234C>G
ENST00000491060.1:n.798C>G
NM_005879.2:c.*234C>G NP_005870.2:n.*234C>G
XM_011533264.1:c.*234C>G XP_011531566.1:n.*234C>G
XM_017005526.1:c.*234C>G XP_016861015.1:n.*234C>G
XR_001739979.1:n.1848C>G
NM_005879.3:c.*234C>G MANE Select NP_005870.2:n.*234C>G