Canonical Allele Identifier: CA390655898

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92005194G>A , CM000676.2:g.92005194G>A	GRCh38
NC_000014.8:g.92471538G>A , CM000676.1:g.92471538G>A	GRCh37
NC_000014.7:g.91541291G>A	NCBI36
NG_016970.1:g.39866C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.2782C>T MANE Select	NP_004230.2:p.Gln928Ter
ENST00000267622.8:c.2782C>T MANE Select	ENSP00000267622.4:p.Gln928Ter
NM_001321851.1:c.2779C>T	NP_001308780.1:p.Gln927Ter
NM_004239.3:c.2782C>T	NP_004230.2:p.Gln928Ter
ENST00000554357.5:c.1928C>T
XM_005268214.2:c.1456C>T	XP_005268271.1:p.Gln486Ter
XM_005268215.2:c.1527+2446C>T	XP_005268272.1:n.1527+2446C>T
XM_006720321.2:c.2779C>T	XP_006720384.1:p.Gln927Ter
XM_011537361.1:c.2782C>T	XP_011535663.1:p.Gln928Ter
XM_017021787.2:c.2077C>T	XP_016877276.1:p.Gln693Ter
XM_017021788.2:c.1456C>T	XP_016877277.1:p.Gln486Ter
XR_001750598.2:n.3231C>T
XR_943560.1:n.3237C>T
XR_943560.2:n.3231C>T