Canonical Allele Identifier: CA390651363

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92004159T>G , CM000676.2:g.92004159T>G	GRCh38
NC_000014.8:g.92470503T>G , CM000676.1:g.92470503T>G	GRCh37
NC_000014.7:g.91540256T>G	NCBI36
NG_016970.1:g.40901A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.3817A>C MANE Select	ENSP00000267622.4:p.Ser1273Arg
ENST00000554357.5:c.2963A>C
NM_004239.3:c.3817A>C	NP_004230.2:p.Ser1273Arg
XM_005268214.2:c.2491A>C	XP_005268271.1:p.Ser831Arg
XM_005268215.2:c.1527+3481A>C	XP_005268272.1:n.1527+3481A>C
XM_006720321.2:c.3814A>C	XP_006720384.1:p.Ser1272Arg
XM_011537361.1:c.3817A>C	XP_011535663.1:p.Ser1273Arg
XR_943560.1:n.4272A>C
NM_001321851.1:c.3814A>C	NP_001308780.1:p.Ser1272Arg
NM_004239.4:c.3817A>C MANE Select	NP_004230.2:p.Ser1273Arg
XM_017021787.2:c.3112A>C	XP_016877276.1:p.Ser1038Arg
XM_017021788.2:c.2491A>C	XP_016877277.1:p.Ser831Arg
XR_001750598.2:n.4266A>C
XR_943560.2:n.4266A>C