Canonical Allele Identifier: CA7609312

Gene: TRIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64394102C>T , CM000677.2:g.64394102C>T	GRCh38
NC_000015.9:g.64686301C>T , CM000677.1:g.64686301C>T	GRCh37
NC_000015.8:g.62473354C>T	NCBI36
NG_046848.1:g.11299C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261884.8:c.258C>T MANE Select	ENSP00000261884.3:p.Cys86=
ENST00000261884.7:c.258C>T	ENSP00000261884.3:p.Cys86=
ENST00000557834.5:n.309C>T
ENST00000558820.5:c.*65C>T	ENSP00000452675.1:n.*65C>T
ENST00000559565.5:n.132C>T
ENST00000559833.5:n.334C>T
ENST00000560567.5:c.258C>T	ENSP00000453106.1:p.Cys86=
ENST00000560920.6:c.258C>T	ENSP00000453276.2:p.Cys86=
ENST00000561265.1:n.407C>T
NM_016213.4:c.258C>T	NP_057297.2:p.Cys86=
XM_005254789.1:c.-433C>T	XP_005254846.1:n.-433C>T
XR_243130.1:n.316C>T
NM_001321924.1:c.-433C>T	NP_001308853.1:n.-433C>T
NR_135855.1:n.318C>T
NM_001321924.2:c.-433C>T	NP_001308853.1:n.-433C>T
NM_016213.5:c.258C>T MANE Select	NP_057297.2:p.Cys86=
NR_135855.2:n.286C>T