Canonical Allele Identifier: CA7313503

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92003770T>C , CM000676.2:g.92003770T>C	GRCh38
NC_000014.8:g.92470114T>C , CM000676.1:g.92470114T>C	GRCh37
NC_000014.7:g.91539867T>C	NCBI36
NG_016970.1:g.41290A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.4206A>G MANE Select	NP_004230.2:p.Gln1402=
ENST00000267622.8:c.4206A>G MANE Select	ENSP00000267622.4:p.Gln1402=
NM_001321851.1:c.4203A>G	NP_001308780.1:p.Gln1401=
NM_004239.3:c.4206A>G	NP_004230.2:p.Gln1402=
ENST00000554357.5:c.3352A>G
XM_005268214.2:c.2880A>G	XP_005268271.1:p.Gln960=
XM_005268215.2:c.1528-3662A>G	XP_005268272.1:n.1528-3662A>G
XM_006720321.2:c.4203A>G	XP_006720384.1:p.Gln1401=
XM_011537361.1:c.4206A>G	XP_011535663.1:p.Gln1402=
XM_017021787.2:c.3501A>G	XP_016877276.1:p.Gln1167=
XM_017021788.2:c.2880A>G	XP_016877277.1:p.Gln960=
XR_001750598.2:n.4655A>G
XR_943560.1:n.4661A>G
XR_943560.2:n.4655A>G