Canonical Allele Identifier: CA709979128

Gene: TRIP11

Linked Data

• dbSNP Id: rs1414431504
• gnomAD v3: 14-91993549-C-T
• gnomAD v4: 14-91993549-C-T
• MyVariant Identifiers: chr14:g.92459893C>T (hg19) ; chr14:g.91993549C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91993549C>T , CM000676.2:g.91993549C>T	GRCh38
NC_000014.8:g.92459893C>T , CM000676.1:g.92459893C>T	GRCh37
NC_000014.7:g.91529646C>T	NCBI36
NG_016970.1:g.51511G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.5160+260G>A MANE Select	ENSP00000267622.4:n.5160+260G>A
ENST00000554357.5:c.4306+260G>A
ENST00000557017.1:c.408+260G>A	ENSP00000451607.1:n.408+260G>A
NM_004239.3:c.5160+260G>A	NP_004230.2:n.5160+260G>A
XM_005268214.2:c.3834+260G>A	XP_005268271.1:n.3834+260G>A
XM_005268215.2:c.2130+260G>A	XP_005268272.1:n.2130+260G>A
XM_006720321.2:c.5157+260G>A	XP_006720384.1:n.5157+260G>A
XR_943560.1:n.5615+260G>A
NM_001321851.1:c.5157+260G>A	NP_001308780.1:n.5157+260G>A
NM_004239.4:c.5160+260G>A MANE Select	NP_004230.2:n.5160+260G>A
XM_017021787.2:c.4455+260G>A	XP_016877276.1:n.4455+260G>A
XM_017021788.2:c.3834+260G>A	XP_016877277.1:n.3834+260G>A
XR_001750598.2:n.5445+260G>A
XR_943560.2:n.5609+260G>A