Canonical Allele Identifier: CA226490422
Gene: MED17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.93807342A>G , CM000673.2:g.93807342A>G GRCh38
NC_000011.9:g.93540508A>G , CM000673.1:g.93540508A>G GRCh37
NC_000011.8:g.93180156A>G NCBI36
NG_028028.1:g.28104A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251871.9:c.1467-176A>G MANE Select ENSP00000251871.3:n.1467-176A>G
ENST00000507258.4:n.3180-176A>G
ENST00000525026.6:n.1774-159A>G
ENST00000525613.2:n.1313-176A>G
ENST00000529626.2:n.1470-176A>G
ENST00000533133.6:c.1467-2375A>G ENSP00000433090.2:n.1467-2375A>G
ENST00000638270.1:n.1242A>G
ENST00000638487.1:c.*793-176A>G ENSP00000492294.1:n.*793-176A>G
ENST00000638518.1:c.492-176A>G
ENST00000638767.1:c.2028-176A>G ENSP00000492220.1:n.2028-176A>G
ENST00000638790.1:c.1310-176A>G ENSP00000491457.1:n.1310-176A>G
ENST00000639189.1:c.*121-176A>G ENSP00000491770.1:n.*121-176A>G
ENST00000639457.1:c.*470-176A>G ENSP00000492391.1:n.*470-176A>G
ENST00000639523.1:c.1402-176A>G
ENST00000639596.1:c.*121-176A>G ENSP00000491918.1:n.*121-176A>G
ENST00000639724.1:c.1467-176A>G ENSP00000492625.1:n.1467-176A>G
ENST00000640027.1:c.1467-159A>G ENSP00000492872.1:n.1467-159A>G
ENST00000640077.1:c.1475-176A>G ENSP00000490968.1:n.1475-176A>G
ENST00000640411.1:n.425-176A>G
ENST00000640451.1:c.1314-176A>G ENSP00000492530.1:n.1314-176A>G
ENST00000640521.1:c.1329-176A>G ENSP00000491108.1:n.1329-176A>G
ENST00000640583.1:n.2030-176A>G
ENST00000640804.1:n.1840-176A>G
ENST00000251871.7:c.1467-176A>G ENSP00000251871.3:n.1467-176A>G
ENST00000525613.1:n.1892-176A>G
ENST00000531920.5:n.768-176A>G
ENST00000533133.5:c.*1009-4482A>G ENSP00000433090.1:n.*1009-4482A>G
ENST00000533367.5:n.520-176A>G
NM_004268.4:c.1467-176A>G NP_004259.3:n.1467-176A>G
XM_011543068.1:c.1467-176A>G XP_011541370.1:n.1467-176A>G
XR_247218.1:n.1516-176A>G
XR_947872.1:n.1701-159A>G
NM_004268.5:c.1467-176A>G MANE Select NP_004259.3:n.1467-176A>G