Canonical Allele Identifier: CA201457

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91974722C>T , CM000676.2:g.91974722C>T	GRCh38
NC_000014.8:g.92441066C>T , CM000676.1:g.92441066C>T	GRCh37
NC_000014.7:g.91510819C>T	NCBI36
NG_016970.1:g.70338G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.5479G>A MANE Select	NP_004230.2:p.Gly1827Ser
ENST00000267622.8:c.5479G>A MANE Select	ENSP00000267622.4:p.Gly1827Ser
NM_001321851.1:c.5476G>A	NP_001308780.1:p.Gly1826Ser
NM_004239.3:c.5479G>A	NP_004230.2:p.Gly1827Ser
ENST00000554357.5:c.4625G>A
XM_005268214.2:c.4153G>A	XP_005268271.1:p.Gly1385Ser
XM_005268215.2:c.2449G>A	XP_005268272.1:p.Gly817Ser
XM_006720321.2:c.5476G>A	XP_006720384.1:p.Gly1826Ser
XM_017021787.2:c.4774G>A	XP_016877276.1:p.Gly1592Ser
XM_017021788.2:c.4153G>A	XP_016877277.1:p.Gly1385Ser
XR_943560.1:n.6057G>A
XR_943560.2:n.6051G>A