Canonical Allele Identifier: CA2574951130
Gene: MED17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.93784723del , CM000673.2:g.93784723del GRCh38
NC_000011.9:g.93517889del , CM000673.1:g.93517889del GRCh37
NC_000011.8:g.93157537del NCBI36
NG_028028.1:g.5485del

Transcript Alleles

HGVS Amino-acid Change
ENST00000251871.9:c.210del MANE Select ENSP00000251871.3:p.Trp70CysfsTer17
ENST00000507258.4:n.298del
ENST00000525026.6:n.431del
ENST00000528786.2:c.150del ENSP00000433626.2:p.Trp50CysfsTer?
ENST00000533133.6:c.210del ENSP00000433090.2:p.Trp70CysfsTer17
ENST00000638294.1:c.210del ENSP00000491675.1:p.Trp70CysfsTer26
ENST00000638487.1:c.210del ENSP00000492294.1:p.Trp70CysfsTer17
ENST00000638518.1:c.146del
ENST00000638767.1:c.771del ENSP00000492220.1:p.Trp257CysfsTer17
ENST00000638790.1:c.48del ENSP00000491457.1:p.Trp16CysfsTer17
ENST00000639189.1:c.210del ENSP00000491770.1:p.Trp70CysfsTer17
ENST00000639457.1:c.210del ENSP00000492391.1:p.Trp70CysfsTer17
ENST00000639596.1:c.210del ENSP00000491918.1:p.Trp70CysfsTer17
ENST00000639724.1:c.210del ENSP00000492625.1:p.Trp70CysfsTer17
ENST00000640027.1:c.210del ENSP00000492872.1:p.Trp70CysfsTer17
ENST00000640451.1:c.210del ENSP00000492530.1:p.Trp70CysfsTer17
ENST00000640473.1:c.210del ENSP00000491371.1:p.Trp70CysfsTer?
ENST00000640521.1:c.210del ENSP00000491108.1:p.Trp70CysfsTer17
ENST00000640583.1:n.497del
ENST00000640804.1:n.497del
ENST00000251871.7:c.210del ENSP00000251871.3:p.Trp70CysfsTer17
ENST00000530819.1:c.210del ENSP00000434459.1:p.Trp70CysfsTer17
ENST00000533133.5:c.210del ENSP00000433090.1:p.Trp70CysfsTer17
ENST00000533359.5:c.210del ENSP00000431524.1:p.Trp70CysfsTer17
NM_004268.4:c.210del NP_004259.3:p.Trp70CysfsTer17
XM_011543068.1:c.210del XP_011541370.1:p.Trp70CysfsTer17
XR_247218.1:n.444del
XR_947872.1:n.444del
NM_004268.5:c.210del MANE Select NP_004259.3:p.Trp70CysfsTer17