Canonical Allele Identifier: CA7313639

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92004596G>A , CM000676.2:g.92004596G>A	GRCh38
NC_000014.8:g.92470940G>A , CM000676.1:g.92470940G>A	GRCh37
NC_000014.7:g.91540693G>A	NCBI36
NG_016970.1:g.40464C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.3380C>T MANE Select	ENSP00000267622.4:p.Ala1127Val
ENST00000554357.5:c.2526C>T
NM_004239.3:c.3380C>T	NP_004230.2:p.Ala1127Val
XM_005268214.2:c.2054C>T	XP_005268271.1:p.Ala685Val
XM_005268215.2:c.1527+3044C>T	XP_005268272.1:n.1527+3044C>T
XM_006720321.2:c.3377C>T	XP_006720384.1:p.Ala1126Val
XM_011537361.1:c.3380C>T	XP_011535663.1:p.Ala1127Val
XR_943560.1:n.3835C>T
NM_001321851.1:c.3377C>T	NP_001308780.1:p.Ala1126Val
NM_004239.4:c.3380C>T MANE Select	NP_004230.2:p.Ala1127Val
XM_017021787.2:c.2675C>T	XP_016877276.1:p.Ala892Val
XM_017021788.2:c.2054C>T	XP_016877277.1:p.Ala685Val
XR_001750598.2:n.3829C>T
XR_943560.2:n.3829C>T