Canonical Allele Identifier: CA7313360

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91999320A>G , CM000676.2:g.91999320A>G	GRCh38
NC_000014.8:g.92465664A>G , CM000676.1:g.92465664A>G	GRCh37
NC_000014.7:g.91535417A>G	NCBI36
NG_016970.1:g.45740T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.4812T>C MANE Select	ENSP00000267622.4:p.Asp1604=
ENST00000554357.5:c.3958T>C
ENST00000557017.1:c.60T>C	ENSP00000451607.1:p.Asp20=
NM_004239.3:c.4812T>C	NP_004230.2:p.Asp1604=
XM_005268214.2:c.3486T>C	XP_005268271.1:p.Asp1162=
XM_005268215.2:c.1782T>C	XP_005268272.1:p.Asp594=
XM_006720321.2:c.4809T>C	XP_006720384.1:p.Asp1603=
XM_011537361.1:c.4812T>C	XP_011535663.1:p.Asp1604=
XR_943560.1:n.5267T>C
NM_001321851.1:c.4809T>C	NP_001308780.1:p.Asp1603=
NM_004239.4:c.4812T>C MANE Select	NP_004230.2:p.Asp1604=
XM_017021787.2:c.4107T>C	XP_016877276.1:p.Asp1369=
XM_017021788.2:c.3486T>C	XP_016877277.1:p.Asp1162=
XR_001750598.2:n.5261T>C
XR_943560.2:n.5261T>C