Canonical Allele Identifier: CA271405479
Gene: TRIP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64413951G>A , CM000677.2:g.64413951G>A GRCh38
NC_000015.9:g.64706150G>A , CM000677.1:g.64706150G>A GRCh37
NC_000015.8:g.62493203G>A NCBI36
NG_046848.1:g.31148G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261884.8:c.1044-134G>A MANE Select ENSP00000261884.3:n.1044-134G>A
ENST00000261884.7:c.1044-134G>A ENSP00000261884.3:n.1044-134G>A
ENST00000560475.1:c.111+4123G>A
ENST00000560567.5:c.1043+4123G>A ENSP00000453106.1:n.1043+4123G>A
NM_016213.4:c.1044-134G>A NP_057297.2:n.1044-134G>A
XM_005254789.1:c.354-134G>A XP_005254846.1:n.354-134G>A
XR_243130.1:n.1101+4123G>A
NM_001321924.1:c.354-134G>A NP_001308853.1:n.354-134G>A
NR_135855.1:n.1103+4123G>A
NM_001321924.2:c.354-134G>A NP_001308853.1:n.354-134G>A
NM_016213.5:c.1044-134G>A MANE Select NP_057297.2:n.1044-134G>A
NR_135855.2:n.1071+4123G>A