Canonical Allele Identifier: CA7313032

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91969724C>T , CM000676.2:g.91969724C>T	GRCh38
NC_000014.8:g.92436068C>T , CM000676.1:g.92436068C>T	GRCh37
NC_000014.7:g.91505821C>T	NCBI36
NG_016970.1:g.75336G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.5889G>A MANE Select	ENSP00000267622.4:p.Ala1963=
ENST00000554357.5:c.5035G>A
NM_004239.3:c.5889G>A	NP_004230.2:p.Ala1963=
XM_005268214.2:c.4563G>A	XP_005268271.1:p.Ala1521=
XM_005268215.2:c.2859G>A	XP_005268272.1:p.Ala953=
XM_006720321.2:c.5886G>A	XP_006720384.1:p.Ala1962=
NM_001321851.1:c.5886G>A	NP_001308780.1:p.Ala1962=
NM_004239.4:c.5889G>A MANE Select	NP_004230.2:p.Ala1963=
XM_017021787.2:c.5184G>A	XP_016877276.1:p.Ala1728=
XM_017021788.2:c.4563G>A	XP_016877277.1:p.Ala1521=