Canonical Allele Identifier: CA2183132263

Gene: TRIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64433291T= , CM000677.2:g.64433291T=	GRCh38
NC_000015.9:g.64725490T= , CM000677.1:g.64725490T=	GRCh37
NC_000015.8:g.62512543T=	NCBI36
NG_046848.1:g.50488T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261884.8:c.1575+7660T= MANE Select	ENSP00000261884.3:n.1575+7660T=
ENST00000261884.7:c.1575+7660T=	ENSP00000261884.3:n.1575+7660T=
ENST00000558162.1:c.133+7660T=
ENST00000560475.1:c.112-11715T=
NM_016213.4:c.1575+7660T=	NP_057297.2:n.1575+7660T=
XM_005254789.1:c.885+7660T=	XP_005254846.1:n.885+7660T=
XR_243130.1:n.1506+7660T=
NM_001321924.1:c.885+7660T=	NP_001308853.1:n.885+7660T=
NR_135855.1:n.1508+7660T=
NM_001321924.2:c.885+7660T=	NP_001308853.1:n.885+7660T=
NM_016213.5:c.1575+7660T= MANE Select	NP_057297.2:n.1575+7660T=
NR_135855.2:n.1476+7660T=