Canonical Allele Identifier: CA7313569

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92004118C>T , CM000676.2:g.92004118C>T	GRCh38
NC_000014.8:g.92470462C>T , CM000676.1:g.92470462C>T	GRCh37
NC_000014.7:g.91540215C>T	NCBI36
NG_016970.1:g.40942G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.3858G>A MANE Select	ENSP00000267622.4:p.Gln1286=
ENST00000554357.5:c.3004G>A
NM_004239.3:c.3858G>A	NP_004230.2:p.Gln1286=
XM_005268214.2:c.2532G>A	XP_005268271.1:p.Gln844=
XM_005268215.2:c.1527+3522G>A	XP_005268272.1:n.1527+3522G>A
XM_006720321.2:c.3855G>A	XP_006720384.1:p.Gln1285=
XM_011537361.1:c.3858G>A	XP_011535663.1:p.Gln1286=
XR_943560.1:n.4313G>A
NM_001321851.1:c.3855G>A	NP_001308780.1:p.Gln1285=
NM_004239.4:c.3858G>A MANE Select	NP_004230.2:p.Gln1286=
XM_017021787.2:c.3153G>A	XP_016877276.1:p.Gln1051=
XM_017021788.2:c.2532G>A	XP_016877277.1:p.Gln844=
XR_001750598.2:n.4307G>A
XR_943560.2:n.4307G>A