Canonical Allele Identifier: CA7609443

Gene: TRIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64400851G>A , CM000677.2:g.64400851G>A	GRCh38
NC_000015.9:g.64693050G>A , CM000677.1:g.64693050G>A	GRCh37
NC_000015.8:g.62480103G>A	NCBI36
NG_046848.1:g.18048G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261884.8:c.697+30G>A MANE Select	ENSP00000261884.3:n.697+30G>A
ENST00000261884.7:c.697+30G>A	ENSP00000261884.3:n.697+30G>A
ENST00000558820.5:c.*504+30G>A	ENSP00000452675.1:n.*504+30G>A
ENST00000559565.5:n.571+30G>A
ENST00000560567.5:c.697+30G>A	ENSP00000453106.1:n.697+30G>A
ENST00000561265.1:n.846+30G>A
NM_016213.4:c.697+30G>A	NP_057297.2:n.697+30G>A
XM_005254789.1:c.7+30G>A	XP_005254846.1:n.7+30G>A
XR_243130.1:n.755+30G>A
NM_001321924.1:c.7+30G>A	NP_001308853.1:n.7+30G>A
NR_135855.1:n.757+30G>A
NM_001321924.2:c.7+30G>A	NP_001308853.1:n.7+30G>A
NM_016213.5:c.697+30G>A MANE Select	NP_057297.2:n.697+30G>A
NR_135855.2:n.725+30G>A