Canonical Allele Identifier: CA1363671541
Gene: TRAIP HGNC NCBI

Linked Data

dbSNP Id: rs2081707064
gnomAD v4: 3-49828974-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828974C>A , CM000665.2:g.49828974C>A GRCh38
NC_000003.11:g.49866407C>A , CM000665.1:g.49866407C>A GRCh37
NC_000003.10:g.49841411C>A NCBI36
NG_046695.1:g.32586G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*129G>T MANE Select ENSP00000328203.2:n.*129G>T
ENST00000331456.6:c.*129G>T ENSP00000328203.2:n.*129G>T
ENST00000491060.1:n.693G>T
NM_005879.2:c.*129G>T NP_005870.2:n.*129G>T
XM_011533264.1:c.*129G>T XP_011531566.1:n.*129G>T
XM_017005526.1:c.*129G>T XP_016861015.1:n.*129G>T
XR_001739979.1:n.1743G>T
NM_005879.3:c.*129G>T MANE Select NP_005870.2:n.*129G>T