Canonical Allele Identifier: CA7609338

Gene: TRIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64395424G>A , CM000677.2:g.64395424G>A	GRCh38
NC_000015.9:g.64687623G>A , CM000677.1:g.64687623G>A	GRCh37
NC_000015.8:g.62474676G>A	NCBI36
NG_046848.1:g.12621G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016213.5:c.298G>A MANE Select	NP_057297.2:p.Asp100Asn
ENST00000261884.8:c.298G>A MANE Select	ENSP00000261884.3:p.Asp100Asn
NM_001321924.1:c.-393G>A	NP_001308853.1:n.-393G>A
NM_001321924.2:c.-393G>A	NP_001308853.1:n.-393G>A
NM_016213.4:c.298G>A	NP_057297.2:p.Asp100Asn
NR_135855.1:n.358G>A
NR_135855.2:n.326G>A
ENST00000261884.7:c.298G>A	ENSP00000261884.3:p.Asp100Asn
ENST00000557834.5:n.349G>A
ENST00000558820.5:c.*105G>A	ENSP00000452675.1:n.*105G>A
ENST00000559565.5:n.172G>A
ENST00000559833.5:n.374G>A
ENST00000560567.5:c.298G>A	ENSP00000453106.1:p.Asp100Asn
ENST00000560920.6:c.271+1309G>A	ENSP00000453276.2:n.271+1309G>A
ENST00000561265.1:n.447G>A
XM_005254789.1:c.-393G>A	XP_005254846.1:n.-393G>A
XR_243130.1:n.356G>A