Canonical Allele Identifier: CA7313861

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92006072G>C , CM000676.2:g.92006072G>C	GRCh38
NC_000014.8:g.92472416G>C , CM000676.1:g.92472416G>C	GRCh37
NC_000014.7:g.91542169G>C	NCBI36
NG_016970.1:g.38988C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.1904C>G MANE Select	ENSP00000267622.4:p.Ser635Cys
ENST00000554357.5:c.1050C>G
NM_004239.3:c.1904C>G	NP_004230.2:p.Ser635Cys
XM_005268214.2:c.578C>G	XP_005268271.1:p.Ser193Cys
XM_005268215.2:c.1527+1568C>G	XP_005268272.1:n.1527+1568C>G
XM_006720321.2:c.1901C>G	XP_006720384.1:p.Ser634Cys
XM_011537361.1:c.1904C>G	XP_011535663.1:p.Ser635Cys
XR_943560.1:n.2359C>G
NM_001321851.1:c.1901C>G	NP_001308780.1:p.Ser634Cys
NM_004239.4:c.1904C>G MANE Select	NP_004230.2:p.Ser635Cys
XM_017021787.2:c.1199C>G	XP_016877276.1:p.Ser400Cys
XM_017021788.2:c.578C>G	XP_016877277.1:p.Ser193Cys
XR_001750598.2:n.2353C>G
XR_943560.2:n.2353C>G