Canonical Allele Identifier: CA390656826

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92005373T>C , CM000676.2:g.92005373T>C	GRCh38
NC_000014.8:g.92471717T>C , CM000676.1:g.92471717T>C	GRCh37
NC_000014.7:g.91541470T>C	NCBI36
NG_016970.1:g.39687A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.2603A>G MANE Select	NP_004230.2:p.Glu868Gly
ENST00000267622.8:c.2603A>G MANE Select	ENSP00000267622.4:p.Glu868Gly
NM_001321851.1:c.2600A>G	NP_001308780.1:p.Glu867Gly
NM_004239.3:c.2603A>G	NP_004230.2:p.Glu868Gly
ENST00000554357.5:c.1749A>G
XM_005268214.2:c.1277A>G	XP_005268271.1:p.Glu426Gly
XM_005268215.2:c.1527+2267A>G	XP_005268272.1:n.1527+2267A>G
XM_006720321.2:c.2600A>G	XP_006720384.1:p.Glu867Gly
XM_011537361.1:c.2603A>G	XP_011535663.1:p.Glu868Gly
XM_017021787.2:c.1898A>G	XP_016877276.1:p.Glu633Gly
XM_017021788.2:c.1277A>G	XP_016877277.1:p.Glu426Gly
XR_001750598.2:n.3052A>G
XR_943560.1:n.3058A>G
XR_943560.2:n.3052A>G