Canonical Allele Identifier: CA7313420

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92000126T>G , CM000676.2:g.92000126T>G	GRCh38
NC_000014.8:g.92466470T>G , CM000676.1:g.92466470T>G	GRCh37
NC_000014.7:g.91536223T>G	NCBI36
NG_016970.1:g.44934A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.4558-18A>C MANE Select	ENSP00000267622.4:n.4558-18A>C
ENST00000554357.5:c.3704-18A>C
NM_004239.3:c.4558-18A>C	NP_004230.2:n.4558-18A>C
XM_005268214.2:c.3232-18A>C	XP_005268271.1:n.3232-18A>C
XM_005268215.2:c.1528-18A>C	XP_005268272.1:n.1528-18A>C
XM_006720321.2:c.4555-18A>C	XP_006720384.1:n.4555-18A>C
XM_011537361.1:c.4558-18A>C	XP_011535663.1:n.4558-18A>C
XR_943560.1:n.5013-18A>C
NM_001321851.1:c.4555-18A>C	NP_001308780.1:n.4555-18A>C
NM_004239.4:c.4558-18A>C MANE Select	NP_004230.2:n.4558-18A>C
XM_017021787.2:c.3853-18A>C	XP_016877276.1:n.3853-18A>C
XM_017021788.2:c.3232-18A>C	XP_016877277.1:n.3232-18A>C
XR_001750598.2:n.5007-18A>C
XR_943560.2:n.5007-18A>C