Canonical Allele Identifier: CA7313424

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92000154_92000155dup , CM000676.2:g.92000154_92000155dup	GRCh38
NC_000014.8:g.92466498_92466499dup , CM000676.1:g.92466498_92466499dup	GRCh37
NC_000014.7:g.91536251_91536252dup	NCBI36
NG_016970.1:g.44918_44919dup

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.4558-34_4558-33dup MANE Select	NP_004230.2:n.4558-34_4558-33dup
ENST00000267622.8:c.4558-34_4558-33dup MANE Select	ENSP00000267622.4:n.4558-34_4558-33dup
NM_001321851.1:c.4555-34_4555-33dup	NP_001308780.1:n.4555-34_4555-33dup
NM_004239.3:c.4558-34_4558-33dup	NP_004230.2:n.4558-34_4558-33dup
ENST00000554357.5:c.3704-34_3704-33dup
XM_005268214.2:c.3232-34_3232-33dup	XP_005268271.1:n.3232-34_3232-33dup
XM_005268215.2:c.1528-34_1528-33dup	XP_005268272.1:n.1528-34_1528-33dup
XM_006720321.2:c.4555-34_4555-33dup	XP_006720384.1:n.4555-34_4555-33dup
XM_011537361.1:c.4558-34_4558-33dup	XP_011535663.1:n.4558-34_4558-33dup
XM_017021787.2:c.3853-34_3853-33dup	XP_016877276.1:n.3853-34_3853-33dup
XM_017021788.2:c.3232-34_3232-33dup	XP_016877277.1:n.3232-34_3232-33dup
XR_001750598.2:n.5007-34_5007-33dup
XR_943560.1:n.5013-34_5013-33dup
XR_943560.2:n.5007-34_5007-33dup