Canonical Allele Identifier: CA7609378

Gene: TRIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64397627G>A , CM000677.2:g.64397627G>A	GRCh38
NC_000015.9:g.64689826G>A , CM000677.1:g.64689826G>A	GRCh37
NC_000015.8:g.62476879G>A	NCBI36
NG_046848.1:g.14824G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261884.8:c.427G>A MANE Select	ENSP00000261884.3:p.Val143Ile
ENST00000261884.7:c.427G>A	ENSP00000261884.3:p.Val143Ile
ENST00000557834.5:n.478G>A
ENST00000558820.5:c.*234G>A	ENSP00000452675.1:n.*234G>A
ENST00000559565.5:n.301G>A
ENST00000559833.5:n.503G>A
ENST00000560567.5:c.427G>A	ENSP00000453106.1:p.Val143Ile
ENST00000560920.6:c.293G>A	ENSP00000453276.2:p.Arg98His
ENST00000561265.1:n.576G>A
NM_016213.4:c.427G>A	NP_057297.2:p.Val143Ile
XM_005254789.1:c.-264G>A	XP_005254846.1:n.-264G>A
XR_243130.1:n.485G>A
NM_001321924.1:c.-264G>A	NP_001308853.1:n.-264G>A
NR_135855.1:n.487G>A
NM_001321924.2:c.-264G>A	NP_001308853.1:n.-264G>A
NM_016213.5:c.427G>A MANE Select	NP_057297.2:p.Val143Ile
NR_135855.2:n.455G>A