Canonical Allele Identifier: CA153674

Gene: MED17

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.93797651A>G , CM000673.2:g.93797651A>G	GRCh38
NC_000011.9:g.93530817A>G , CM000673.1:g.93530817A>G	GRCh37
NC_000011.8:g.93170465A>G	NCBI36
NG_028028.1:g.18413A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251871.9:c.1260A>G MANE Select	ENSP00000251871.3:p.Ser420=
ENST00000507258.4:n.2973A>G
ENST00000525026.6:n.1567A>G
ENST00000529626.2:n.1263A>G
ENST00000531920.6:n.561A>G
ENST00000533133.6:c.1260A>G	ENSP00000433090.2:p.Ser420=
ENST00000533367.6:n.298A>G
ENST00000638487.1:c.*586A>G	ENSP00000492294.1:n.*586A>G
ENST00000638518.1:c.354-4184A>G
ENST00000638767.1:c.1821A>G	ENSP00000492220.1:p.Ser607=
ENST00000638790.1:c.1171+1111A>G	ENSP00000491457.1:n.1171+1111A>G
ENST00000639189.1:c.1143+1111A>G	ENSP00000491770.1:n.1143+1111A>G
ENST00000639457.1:c.*469+1111A>G	ENSP00000492391.1:n.*469+1111A>G
ENST00000639523.1:c.1195A>G
ENST00000639596.1:c.1143+1111A>G	ENSP00000491918.1:n.1143+1111A>G
ENST00000639724.1:c.1260A>G	ENSP00000492625.1:p.Ser420=
ENST00000640027.1:c.1260A>G	ENSP00000492872.1:p.Ser420=
ENST00000640077.1:c.1268A>G	ENSP00000490968.1:n.1268A>G
ENST00000640451.1:c.1107A>G	ENSP00000492530.1:p.Ser369=
ENST00000640473.1:c.*109A>G	ENSP00000491371.1:n.*109A>G
ENST00000640521.1:c.1260A>G	ENSP00000491108.1:p.Ser420=
ENST00000640583.1:n.1823A>G
ENST00000640804.1:n.1633A>G
ENST00000251871.7:c.1260A>G	ENSP00000251871.3:p.Ser420=
ENST00000531920.5:n.561A>G
ENST00000533133.5:c.*545A>G	ENSP00000433090.1:n.*545A>G
ENST00000533367.5:n.313A>G
NM_004268.4:c.1260A>G	NP_004259.3:p.Ser420=
XM_011543068.1:c.1260A>G	XP_011541370.1:p.Ser420=
XR_247218.1:n.1377+1111A>G
XR_947872.1:n.1494A>G
NM_004268.5:c.1260A>G MANE Select	NP_004259.3:p.Ser420=