Canonical Allele Identifier: CA392818963

Gene: TRIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64397734C>A , CM000677.2:g.64397734C>A	GRCh38
NC_000015.9:g.64689933C>A , CM000677.1:g.64689933C>A	GRCh37
NC_000015.8:g.62476986C>A	NCBI36
NG_046848.1:g.14931C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016213.5:c.534C>A MANE Select	NP_057297.2:p.His178Gln
ENST00000261884.8:c.534C>A MANE Select	ENSP00000261884.3:p.His178Gln
NM_001321924.1:c.-157C>A	NP_001308853.1:n.-157C>A
NM_001321924.2:c.-157C>A	NP_001308853.1:n.-157C>A
NM_016213.4:c.534C>A	NP_057297.2:p.His178Gln
NR_135855.1:n.594C>A
NR_135855.2:n.562C>A
ENST00000261884.7:c.534C>A	ENSP00000261884.3:p.His178Gln
ENST00000557834.5:n.585C>A
ENST00000558820.5:c.*341C>A	ENSP00000452675.1:n.*341C>A
ENST00000559565.5:n.408C>A
ENST00000559833.5:n.610C>A
ENST00000560567.5:c.534C>A	ENSP00000453106.1:p.His178Gln
ENST00000560920.6:c.*19C>A	ENSP00000453276.2:n.*19C>A
ENST00000561265.1:n.683C>A
XM_005254789.1:c.-157C>A	XP_005254846.1:n.-157C>A
XR_243130.1:n.592C>A