Canonical Allele Identifier: CA271402950

Gene: TRIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64409500_64409501del , CM000677.2:g.64409500_64409501del	GRCh38
NC_000015.9:g.64701699_64701700del , CM000677.1:g.64701699_64701700del	GRCh37
NC_000015.8:g.62488752_62488753del	NCBI36
NG_046848.1:g.26697_26698del

Transcript Alleles

HGVS	Amino-acid Change
NM_016213.5:c.828-113_828-112del MANE Select	NP_057297.2:n.828-113_828-112del
ENST00000261884.8:c.828-113_828-112del MANE Select	ENSP00000261884.3:n.828-113_828-112del
NM_001321924.1:c.138-113_138-112del	NP_001308853.1:n.138-113_138-112del
NM_001321924.2:c.138-113_138-112del	NP_001308853.1:n.138-113_138-112del
NM_016213.4:c.828-113_828-112del	NP_057297.2:n.828-113_828-112del
NR_135855.1:n.888-113_888-112del
NR_135855.2:n.856-113_856-112del
ENST00000261884.7:c.828-113_828-112del	ENSP00000261884.3:n.828-113_828-112del
ENST00000558820.5:c.*635-113_*635-112del	ENSP00000452675.1:n.*635-113_*635-112del
ENST00000559565.5:n.572-113_572-112del
ENST00000560567.5:c.828-113_828-112del	ENSP00000453106.1:n.828-113_828-112del
ENST00000561265.1:n.847-113_847-112del
XM_005254789.1:c.138-113_138-112del	XP_005254846.1:n.138-113_138-112del
XR_243130.1:n.886-113_886-112del