Canonical Allele Identifier: CA7609272
Gene: TRIP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64387898T>G , CM000677.2:g.64387898T>G GRCh38
NC_000015.9:g.64680097T>G , CM000677.1:g.64680097T>G GRCh37
NC_000015.8:g.62467150T>G NCBI36
NG_046848.1:g.5095T>G

Transcript Alleles

HGVS Amino-acid Change
NM_016213.5:c.35T>G MANE Select NP_057297.2:p.Leu12Arg
ENST00000261884.8:c.35T>G MANE Select ENSP00000261884.3:p.Leu12Arg
NM_001321924.1:c.-740T>G NP_001308853.1:n.-740T>G
NM_001321924.2:c.-740T>G NP_001308853.1:n.-740T>G
NM_016213.4:c.35T>G NP_057297.2:p.Leu12Arg
NR_135855.1:n.95T>G
NR_135855.2:n.63T>G
ENST00000261884.7:c.35T>G ENSP00000261884.3:p.Leu12Arg
ENST00000557834.5:n.63T>G
ENST00000558442.1:n.37T>G
ENST00000558820.5:c.35T>G ENSP00000452675.1:p.Leu12Arg
ENST00000559565.5:n.36+110T>G
ENST00000559833.5:n.41+110T>G
ENST00000560567.5:c.35T>G ENSP00000453106.1:p.Leu12Arg
ENST00000560920.6:c.35T>G ENSP00000453276.2:p.Leu12Arg
XM_005254789.1:c.-740T>G XP_005254846.1:n.-740T>G
XR_243130.1:n.93T>G