Canonical Allele Identifier: CA7313631

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92004545G>A , CM000676.2:g.92004545G>A	GRCh38
NC_000014.8:g.92470889G>A , CM000676.1:g.92470889G>A	GRCh37
NC_000014.7:g.91540642G>A	NCBI36
NG_016970.1:g.40515C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.3431C>T MANE Select	ENSP00000267622.4:p.Ser1144Phe
ENST00000554357.5:c.2577C>T
NM_004239.3:c.3431C>T	NP_004230.2:p.Ser1144Phe
XM_005268214.2:c.2105C>T	XP_005268271.1:p.Ser702Phe
XM_005268215.2:c.1527+3095C>T	XP_005268272.1:n.1527+3095C>T
XM_006720321.2:c.3428C>T	XP_006720384.1:p.Ser1143Phe
XM_011537361.1:c.3431C>T	XP_011535663.1:p.Ser1144Phe
XR_943560.1:n.3886C>T
NM_001321851.1:c.3428C>T	NP_001308780.1:p.Ser1143Phe
NM_004239.4:c.3431C>T MANE Select	NP_004230.2:p.Ser1144Phe
XM_017021787.2:c.2726C>T	XP_016877276.1:p.Ser909Phe
XM_017021788.2:c.2105C>T	XP_016877277.1:p.Ser702Phe
XR_001750598.2:n.3880C>T
XR_943560.2:n.3880C>T