Canonical Allele Identifier: CA7313089

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91972785T>C , CM000676.2:g.91972785T>C	GRCh38
NC_000014.8:g.92439129T>C , CM000676.1:g.92439129T>C	GRCh37
NC_000014.7:g.91508882T>C	NCBI36
NG_016970.1:g.72275A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.5651A>G MANE Select	ENSP00000267622.4:p.His1884Arg
ENST00000554357.5:c.4797A>G
NM_004239.3:c.5651A>G	NP_004230.2:p.His1884Arg
XM_005268214.2:c.4325A>G	XP_005268271.1:p.His1442Arg
XM_005268215.2:c.2621A>G	XP_005268272.1:p.His874Arg
XM_006720321.2:c.5648A>G	XP_006720384.1:p.His1883Arg
NM_001321851.1:c.5648A>G	NP_001308780.1:p.His1883Arg
NM_004239.4:c.5651A>G MANE Select	NP_004230.2:p.His1884Arg
XM_017021787.2:c.4946A>G	XP_016877276.1:p.His1649Arg
XM_017021788.2:c.4325A>G	XP_016877277.1:p.His1442Arg