Canonical Allele Identifier: CA7313650

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92004670A>G , CM000676.2:g.92004670A>G	GRCh38
NC_000014.8:g.92471014A>G , CM000676.1:g.92471014A>G	GRCh37
NC_000014.7:g.91540767A>G	NCBI36
NG_016970.1:g.40390T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.3306T>C MANE Select	ENSP00000267622.4:p.Phe1102=
ENST00000554357.5:c.2452T>C
NM_004239.3:c.3306T>C	NP_004230.2:p.Phe1102=
XM_005268214.2:c.1980T>C	XP_005268271.1:p.Phe660=
XM_005268215.2:c.1527+2970T>C	XP_005268272.1:n.1527+2970T>C
XM_006720321.2:c.3303T>C	XP_006720384.1:p.Phe1101=
XM_011537361.1:c.3306T>C	XP_011535663.1:p.Phe1102=
XR_943560.1:n.3761T>C
NM_001321851.1:c.3303T>C	NP_001308780.1:p.Phe1101=
NM_004239.4:c.3306T>C MANE Select	NP_004230.2:p.Phe1102=
XM_017021787.2:c.2601T>C	XP_016877276.1:p.Phe867=
XM_017021788.2:c.1980T>C	XP_016877277.1:p.Phe660=
XR_001750598.2:n.3755T>C
XR_943560.2:n.3755T>C