Canonical Allele Identifier: CA7314259
Community Standard Title: NM_004239.4(TRIP11):c.202-11T>G
Gene: TRIP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92025431A>C , CM000676.2:g.92025431A>C GRCh38
NC_000014.8:g.92491775A>C , CM000676.1:g.92491775A>C GRCh37
NC_000014.7:g.91561528A>C NCBI36
NG_016970.1:g.19629T>G

Transcript Alleles

HGVS Amino-acid Change
NM_004239.4:c.202-11T>G MANE Select NP_004230.2:n.202-11T>G
ENST00000267622.8:c.202-11T>G MANE Select ENSP00000267622.4:n.202-11T>G
NM_001321851.1:c.199-11T>G NP_001308780.1:n.199-11T>G
NM_004239.3:c.202-11T>G NP_004230.2:n.202-11T>G
ENST00000555516.6:c.-282-11T>G ENSP00000451944.1:n.-282-11T>G
XM_005268215.2:c.202-11T>G XP_005268272.1:n.202-11T>G
XM_006720321.2:c.199-11T>G XP_006720384.1:n.199-11T>G
XM_011537361.1:c.202-11T>G XP_011535663.1:n.202-11T>G
XM_017021787.2:c.-545-11T>G XP_016877276.1:n.-545-11T>G
XM_017021788.2:c.-997-11T>G XP_016877277.1:n.-997-11T>G
XR_001750598.2:n.651-11T>G
XR_943560.1:n.657-11T>G
XR_943560.2:n.651-11T>G