Canonical Allele Identifier: CA7609594
Gene: TRIP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64418564C>T , CM000677.2:g.64418564C>T GRCh38
NC_000015.9:g.64710763C>T , CM000677.1:g.64710763C>T GRCh37
NC_000015.8:g.62497816C>T NCBI36
NG_046848.1:g.35761C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261884.8:c.1194C>T MANE Select ENSP00000261884.3:p.Ala398=
ENST00000261884.7:c.1194C>T ENSP00000261884.3:p.Ala398=
ENST00000560475.1:c.111+8736C>T
ENST00000560567.5:c.1067C>T ENSP00000453106.1:p.Pro356Leu
NM_016213.4:c.1194C>T NP_057297.2:p.Ala398=
XM_005254789.1:c.504C>T XP_005254846.1:p.Ala168=
XR_243130.1:n.1125C>T
NM_001321924.1:c.504C>T NP_001308853.1:p.Ala168=
NR_135855.1:n.1127C>T
NM_001321924.2:c.504C>T NP_001308853.1:p.Ala168=
NM_016213.5:c.1194C>T MANE Select NP_057297.2:p.Ala398=
NR_135855.2:n.1095C>T