Canonical Allele Identifier: CA271492462

Gene: TRIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64388210A>G , CM000677.2:g.64388210A>G	GRCh38
NC_000015.9:g.64680409A>G , CM000677.1:g.64680409A>G	GRCh37
NC_000015.8:g.62467462A>G	NCBI36
NG_046848.1:g.5407A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261884.8:c.101+246A>G MANE Select	ENSP00000261884.3:n.101+246A>G
ENST00000261884.7:c.101+246A>G	ENSP00000261884.3:n.101+246A>G
ENST00000557834.5:n.213+162A>G
ENST00000558442.1:n.187+162A>G
ENST00000558820.5:c.101+246A>G	ENSP00000452675.1:n.101+246A>G
ENST00000559565.5:n.36+422A>G
ENST00000559833.5:n.41+422A>G
ENST00000560567.5:c.101+246A>G	ENSP00000453106.1:n.101+246A>G
ENST00000560920.6:c.101+246A>G	ENSP00000453276.2:n.101+246A>G
NM_016213.4:c.101+246A>G	NP_057297.2:n.101+246A>G
XM_005254789.1:c.-590+162A>G	XP_005254846.1:n.-590+162A>G
XR_243130.1:n.159+246A>G
NM_001321924.1:c.-590+162A>G	NP_001308853.1:n.-590+162A>G
NR_135855.1:n.161+246A>G
NM_001321924.2:c.-590+162A>G	NP_001308853.1:n.-590+162A>G
NM_016213.5:c.101+246A>G MANE Select	NP_057297.2:n.101+246A>G
NR_135855.2:n.129+246A>G