Canonical Allele Identifier: CA7313096
Community Standard Title: NM_004239.4(TRIP11):c.5607A>G (p.Glu1869=)
Gene: TRIP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91972829T>C , CM000676.2:g.91972829T>C GRCh38
NC_000014.8:g.92439173T>C , CM000676.1:g.92439173T>C GRCh37
NC_000014.7:g.91508926T>C NCBI36
NG_016970.1:g.72231A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004239.4:c.5607A>G MANE Select NP_004230.2:p.Glu1869=
ENST00000267622.8:c.5607A>G MANE Select ENSP00000267622.4:p.Glu1869=
NM_001321851.1:c.5604A>G NP_001308780.1:p.Glu1868=
NM_004239.3:c.5607A>G NP_004230.2:p.Glu1869=
ENST00000554357.5:c.4753A>G
XM_005268214.2:c.4281A>G XP_005268271.1:p.Glu1427=
XM_005268215.2:c.2577A>G XP_005268272.1:p.Glu859=
XM_006720321.2:c.5604A>G XP_006720384.1:p.Glu1868=
XM_017021787.2:c.4902A>G XP_016877276.1:p.Glu1634=
XM_017021788.2:c.4281A>G XP_016877277.1:p.Glu1427=