Canonical Allele Identifier: CA7609565
Community Standard Title: NM_016213.5(TRIP4):c.1170+18C>G
Gene: TRIP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64414229C>G , CM000677.2:g.64414229C>G GRCh38
NC_000015.9:g.64706428C>G , CM000677.1:g.64706428C>G GRCh37
NC_000015.8:g.62493481C>G NCBI36
NG_046848.1:g.31426C>G

Transcript Alleles

HGVS Amino-acid Change
NM_016213.5:c.1170+18C>G MANE Select NP_057297.2:n.1170+18C>G
ENST00000261884.8:c.1170+18C>G MANE Select ENSP00000261884.3:n.1170+18C>G
NM_001321924.1:c.480+18C>G NP_001308853.1:n.480+18C>G
NM_001321924.2:c.480+18C>G NP_001308853.1:n.480+18C>G
NM_016213.4:c.1170+18C>G NP_057297.2:n.1170+18C>G
NR_135855.1:n.1104-4312C>G
NR_135855.2:n.1072-4312C>G
ENST00000261884.7:c.1170+18C>G ENSP00000261884.3:n.1170+18C>G
ENST00000560475.1:c.111+4401C>G
ENST00000560567.5:c.1044-4312C>G ENSP00000453106.1:n.1044-4312C>G
XM_005254789.1:c.480+18C>G XP_005254846.1:n.480+18C>G
XR_243130.1:n.1102-4312C>G