Canonical Allele Identifier: CA2155207376

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91993638C= , CM000676.2:g.91993638C=	GRCh38
NC_000014.8:g.92459982C= , CM000676.1:g.92459982C=	GRCh37
NC_000014.7:g.91529735C=	NCBI36
NG_016970.1:g.51422G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267622.8:c.5160+171G= MANE Select	ENSP00000267622.4:n.5160+171G=
ENST00000554357.5:c.4306+171G=
ENST00000557017.1:c.408+171G=	ENSP00000451607.1:n.408+171G=
NM_004239.3:c.5160+171G=	NP_004230.2:n.5160+171G=
XM_005268214.2:c.3834+171G=	XP_005268271.1:n.3834+171G=
XM_005268215.2:c.2130+171G=	XP_005268272.1:n.2130+171G=
XM_006720321.2:c.5157+171G=	XP_006720384.1:n.5157+171G=
XR_943560.1:n.5615+171G=
NM_001321851.1:c.5157+171G=	NP_001308780.1:n.5157+171G=
NM_004239.4:c.5160+171G= MANE Select	NP_004230.2:n.5160+171G=
XM_017021787.2:c.4455+171G=	XP_016877276.1:n.4455+171G=
XM_017021788.2:c.3834+171G=	XP_016877277.1:n.3834+171G=
XR_001750598.2:n.5445+171G=
XR_943560.2:n.5609+171G=