Canonical Allele Identifier: CA7314183
Gene: TRIP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92021667G>A , CM000676.2:g.92021667G>A GRCh38
NC_000014.8:g.92488011G>A , CM000676.1:g.92488011G>A GRCh37
NC_000014.7:g.91557764G>A NCBI36
NG_016970.1:g.23393C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004239.4:c.477C>T MANE Select NP_004230.2:p.Asp159=
ENST00000267622.8:c.477C>T MANE Select ENSP00000267622.4:p.Asp159=
NM_001321851.1:c.474C>T NP_001308780.1:p.Asp158=
NM_004239.3:c.477C>T NP_004230.2:p.Asp159=
ENST00000555516.6:c.-7C>T ENSP00000451944.1:n.-7C>T
XM_005268215.2:c.477C>T XP_005268272.1:p.Asp159=
XM_006720321.2:c.474C>T XP_006720384.1:p.Asp158=
XM_011537361.1:c.477C>T XP_011535663.1:p.Asp159=
XM_017021787.2:c.-270C>T XP_016877276.1:n.-270C>T
XM_017021788.2:c.-722C>T XP_016877277.1:n.-722C>T
XR_001750598.2:n.926C>T
XR_943560.1:n.932C>T
XR_943560.2:n.926C>T