Canonical Allele Identifier: CA265635505

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91973064C>T , CM000676.2:g.91973064C>T	GRCh38
NC_000014.8:g.92439408C>T , CM000676.1:g.92439408C>T	GRCh37
NC_000014.7:g.91509161C>T	NCBI36
NG_016970.1:g.71996G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.5575-203G>A MANE Select	ENSP00000267622.4:n.5575-203G>A
ENST00000554357.5:c.4721-203G>A
NM_004239.3:c.5575-203G>A	NP_004230.2:n.5575-203G>A
XM_005268214.2:c.4249-203G>A	XP_005268271.1:n.4249-203G>A
XM_005268215.2:c.2545-203G>A	XP_005268272.1:n.2545-203G>A
XM_006720321.2:c.5572-203G>A	XP_006720384.1:n.5572-203G>A
NM_001321851.1:c.5572-203G>A	NP_001308780.1:n.5572-203G>A
NM_004239.4:c.5575-203G>A MANE Select	NP_004230.2:n.5575-203G>A
XM_017021787.2:c.4870-203G>A	XP_016877276.1:n.4870-203G>A
XM_017021788.2:c.4249-203G>A	XP_016877277.1:n.4249-203G>A