Canonical Allele Identifier: CA7313145
Community Standard Title: NM_004239.4(TRIP11):c.5458-43dup
Gene: TRIP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91974798dup , CM000676.2:g.91974798dup GRCh38
NC_000014.8:g.92441142dup , CM000676.1:g.92441142dup GRCh37
NC_000014.7:g.91510895dup NCBI36
NG_016970.1:g.70274dup

Transcript Alleles

HGVS Amino-acid Change
NM_004239.4:c.5458-43dup MANE Select NP_004230.2:n.5458-43dup
ENST00000267622.8:c.5458-43dup MANE Select ENSP00000267622.4:n.5458-43dup
NM_001321851.1:c.5455-43dup NP_001308780.1:n.5455-43dup
NM_004239.3:c.5458-43dup NP_004230.2:n.5458-43dup
ENST00000554357.5:c.4604-43dup
XM_005268214.2:c.4132-43dup XP_005268271.1:n.4132-43dup
XM_005268215.2:c.2428-43dup XP_005268272.1:n.2428-43dup
XM_006720321.2:c.5455-43dup XP_006720384.1:n.5455-43dup
XM_017021787.2:c.4753-43dup XP_016877276.1:n.4753-43dup
XM_017021788.2:c.4132-43dup XP_016877277.1:n.4132-43dup
XR_943560.1:n.6036-43dup
XR_943560.2:n.6030-43dup