Canonical Allele Identifier: CA392821415
Gene: TRIP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64409737C>A , CM000677.2:g.64409737C>A GRCh38
NC_000015.9:g.64701936C>A , CM000677.1:g.64701936C>A GRCh37
NC_000015.8:g.62488989C>A NCBI36
NG_046848.1:g.26934C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261884.8:c.952C>A MANE Select ENSP00000261884.3:p.His318Asn
ENST00000261884.7:c.952C>A ENSP00000261884.3:p.His318Asn
ENST00000559565.5:n.696C>A
ENST00000560475.1:c.20C>A
ENST00000560567.5:c.952C>A ENSP00000453106.1:p.His318Asn
ENST00000561265.1:n.971C>A
NM_016213.4:c.952C>A NP_057297.2:p.His318Asn
XM_005254789.1:c.262C>A XP_005254846.1:p.His88Asn
XR_243130.1:n.1010C>A
NM_001321924.1:c.262C>A NP_001308853.1:p.His88Asn
NR_135855.1:n.1012C>A
NM_001321924.2:c.262C>A NP_001308853.1:p.His88Asn
NM_016213.5:c.952C>A MANE Select NP_057297.2:p.His318Asn
NR_135855.2:n.980C>A