Canonical Allele Identifier: CA390644275

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91974682G>C , CM000676.2:g.91974682G>C	GRCh38
NC_000014.8:g.92441026G>C , CM000676.1:g.92441026G>C	GRCh37
NC_000014.7:g.91510779G>C	NCBI36
NG_016970.1:g.70378C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.5519C>G MANE Select	NP_004230.2:p.Ser1840Ter
ENST00000267622.8:c.5519C>G MANE Select	ENSP00000267622.4:p.Ser1840Ter
NM_001321851.1:c.5516C>G	NP_001308780.1:p.Ser1839Ter
NM_004239.3:c.5519C>G	NP_004230.2:p.Ser1840Ter
ENST00000554357.5:c.4665C>G
XM_005268214.2:c.4193C>G	XP_005268271.1:p.Ser1398Ter
XM_005268215.2:c.2489C>G	XP_005268272.1:p.Ser830Ter
XM_006720321.2:c.5516C>G	XP_006720384.1:p.Ser1839Ter
XM_017021787.2:c.4814C>G	XP_016877276.1:p.Ser1605Ter
XM_017021788.2:c.4193C>G	XP_016877277.1:p.Ser1398Ter