Canonical Allele Identifier: CA2802600219

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91993540G>T , CM000676.2:g.91993540G>T	GRCh38
NC_000014.8:g.92459884G>T , CM000676.1:g.92459884G>T	GRCh37
NC_000014.7:g.91529637G>T	NCBI36
NG_016970.1:g.51520C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.5160+269C>A MANE Select	ENSP00000267622.4:n.5160+269C>A
ENST00000554357.5:c.4306+269C>A
ENST00000557017.1:c.408+269C>A	ENSP00000451607.1:n.408+269C>A
NM_004239.3:c.5160+269C>A	NP_004230.2:n.5160+269C>A
XM_005268214.2:c.3834+269C>A	XP_005268271.1:n.3834+269C>A
XM_005268215.2:c.2130+269C>A	XP_005268272.1:n.2130+269C>A
XM_006720321.2:c.5157+269C>A	XP_006720384.1:n.5157+269C>A
XR_943560.1:n.5615+269C>A
NM_001321851.1:c.5157+269C>A	NP_001308780.1:n.5157+269C>A
NM_004239.4:c.5160+269C>A MANE Select	NP_004230.2:n.5160+269C>A
XM_017021787.2:c.4455+269C>A	XP_016877276.1:n.4455+269C>A
XM_017021788.2:c.3834+269C>A	XP_016877277.1:n.3834+269C>A
XR_001750598.2:n.5445+269C>A
XR_943560.2:n.5609+269C>A