Canonical Allele Identifier: CA965976479

Gene: TRIP11

Linked Data

• dbSNP Id: rs2056709579
• gnomAD v3: 14-91993620-T-G
• gnomAD v4: 14-91993620-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91993620T>G , CM000676.2:g.91993620T>G	GRCh38
NC_000014.8:g.92459964T>G , CM000676.1:g.92459964T>G	GRCh37
NC_000014.7:g.91529717T>G	NCBI36
NG_016970.1:g.51440A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.5160+189A>C MANE Select	ENSP00000267622.4:n.5160+189A>C
ENST00000554357.5:c.4306+189A>C
ENST00000557017.1:c.408+189A>C	ENSP00000451607.1:n.408+189A>C
NM_004239.3:c.5160+189A>C	NP_004230.2:n.5160+189A>C
XM_005268214.2:c.3834+189A>C	XP_005268271.1:n.3834+189A>C
XM_005268215.2:c.2130+189A>C	XP_005268272.1:n.2130+189A>C
XM_006720321.2:c.5157+189A>C	XP_006720384.1:n.5157+189A>C
XR_943560.1:n.5615+189A>C
NM_001321851.1:c.5157+189A>C	NP_001308780.1:n.5157+189A>C
NM_004239.4:c.5160+189A>C MANE Select	NP_004230.2:n.5160+189A>C
XM_017021787.2:c.4455+189A>C	XP_016877276.1:n.4455+189A>C
XM_017021788.2:c.3834+189A>C	XP_016877277.1:n.3834+189A>C
XR_001750598.2:n.5445+189A>C
XR_943560.2:n.5609+189A>C