Canonical Allele Identifier: CA7313926

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92007650T>G , CM000676.2:g.92007650T>G	GRCh38
NC_000014.8:g.92473994T>G , CM000676.1:g.92473994T>G	GRCh37
NC_000014.7:g.91543747T>G	NCBI36
NG_016970.1:g.37410A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.1517A>C MANE Select	ENSP00000267622.4:p.Glu506Ala
ENST00000554357.5:c.663A>C
NM_004239.3:c.1517A>C	NP_004230.2:p.Glu506Ala
XM_005268214.2:c.191A>C	XP_005268271.1:p.Glu64Ala
XM_005268215.2:c.1517A>C	XP_005268272.1:p.Glu506Ala
XM_006720321.2:c.1514A>C	XP_006720384.1:p.Glu505Ala
XM_011537361.1:c.1517A>C	XP_011535663.1:p.Glu506Ala
XR_943560.1:n.1972A>C
NM_001321851.1:c.1514A>C	NP_001308780.1:p.Glu505Ala
NM_004239.4:c.1517A>C MANE Select	NP_004230.2:p.Glu506Ala
XM_017021787.2:c.812A>C	XP_016877276.1:p.Glu271Ala
XM_017021788.2:c.191A>C	XP_016877277.1:p.Glu64Ala
XR_001750598.2:n.1966A>C
XR_943560.2:n.1966A>C