Canonical Allele Identifier: CA265601326

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91995779C>A , CM000676.2:g.91995779C>A	GRCh38
NC_000014.8:g.92462123C>A , CM000676.1:g.92462123C>A	GRCh37
NC_000014.7:g.91531876C>A	NCBI36
NG_016970.1:g.49281G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.4893-264G>T MANE Select	NP_004230.2:n.4893-264G>T
ENST00000267622.8:c.4893-264G>T MANE Select	ENSP00000267622.4:n.4893-264G>T
NM_001321851.1:c.4890-264G>T	NP_001308780.1:n.4890-264G>T
NM_004239.3:c.4893-264G>T	NP_004230.2:n.4893-264G>T
ENST00000554357.5:c.4039-264G>T
ENST00000557017.1:c.141-264G>T	ENSP00000451607.1:n.141-264G>T
XM_005268214.2:c.3567-264G>T	XP_005268271.1:n.3567-264G>T
XM_005268215.2:c.1863-264G>T	XP_005268272.1:n.1863-264G>T
XM_006720321.2:c.4890-264G>T	XP_006720384.1:n.4890-264G>T
XM_011537361.1:c.4893-1867G>T	XP_011535663.1:n.4893-1867G>T
XM_017021787.2:c.4188-264G>T	XP_016877276.1:n.4188-264G>T
XM_017021788.2:c.3567-264G>T	XP_016877277.1:n.3567-264G>T
XR_001750598.2:n.5342-1867G>T
XR_943560.1:n.5348-264G>T
XR_943560.2:n.5342-264G>T