Canonical Allele Identifier: CA14161769

Gene: TRIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64388192C>A , CM000677.2:g.64388192C>A	GRCh38
NC_000015.9:g.64680391C>A , CM000677.1:g.64680391C>A	GRCh37
NC_000015.8:g.62467444C>A	NCBI36
NG_046848.1:g.5389C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016213.5:c.101+228C>A MANE Select	NP_057297.2:n.101+228C>A
ENST00000261884.8:c.101+228C>A MANE Select	ENSP00000261884.3:n.101+228C>A
NM_001321924.1:c.-590+144C>A	NP_001308853.1:n.-590+144C>A
NM_001321924.2:c.-590+144C>A	NP_001308853.1:n.-590+144C>A
NM_016213.4:c.101+228C>A	NP_057297.2:n.101+228C>A
NR_135855.1:n.161+228C>A
NR_135855.2:n.129+228C>A
ENST00000261884.7:c.101+228C>A	ENSP00000261884.3:n.101+228C>A
ENST00000557834.5:n.213+144C>A
ENST00000558442.1:n.187+144C>A
ENST00000558820.5:c.101+228C>A	ENSP00000452675.1:n.101+228C>A
ENST00000559565.5:n.36+404C>A
ENST00000559833.5:n.41+404C>A
ENST00000560567.5:c.101+228C>A	ENSP00000453106.1:n.101+228C>A
ENST00000560920.6:c.101+228C>A	ENSP00000453276.2:n.101+228C>A
XM_005254789.1:c.-590+144C>A	XP_005254846.1:n.-590+144C>A
XR_243130.1:n.159+228C>A