Canonical Allele Identifier: CA7609560
Community Standard Title: NM_016213.5(TRIP4):c.1165C>T (p.Pro389Ser)
Gene: TRIP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64414206C>T , CM000677.2:g.64414206C>T GRCh38
NC_000015.9:g.64706405C>T , CM000677.1:g.64706405C>T GRCh37
NC_000015.8:g.62493458C>T NCBI36
NG_046848.1:g.31403C>T

Transcript Alleles

HGVS Amino-acid Change
NM_016213.5:c.1165C>T MANE Select NP_057297.2:p.Pro389Ser
ENST00000261884.8:c.1165C>T MANE Select ENSP00000261884.3:p.Pro389Ser
NM_001321924.1:c.475C>T NP_001308853.1:p.Pro159Ser
NM_001321924.2:c.475C>T NP_001308853.1:p.Pro159Ser
NM_016213.4:c.1165C>T NP_057297.2:p.Pro389Ser
NR_135855.1:n.1104-4335C>T
NR_135855.2:n.1072-4335C>T
ENST00000261884.7:c.1165C>T ENSP00000261884.3:p.Pro389Ser
ENST00000560475.1:c.111+4378C>T
ENST00000560567.5:c.1044-4335C>T ENSP00000453106.1:n.1044-4335C>T
XM_005254789.1:c.475C>T XP_005254846.1:p.Pro159Ser
XR_243130.1:n.1102-4335C>T