Canonical Allele Identifier: CA226483183

Gene: MED17

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.93797869G>A , CM000673.2:g.93797869G>A	GRCh38
NC_000011.9:g.93531035G>A , CM000673.1:g.93531035G>A	GRCh37
NC_000011.8:g.93170683G>A	NCBI36
NG_028028.1:g.18631G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251871.9:c.1328+150G>A MANE Select	ENSP00000251871.3:n.1328+150G>A
ENST00000507258.4:n.3041+150G>A
ENST00000525026.6:n.1635+150G>A
ENST00000529626.2:n.1331+150G>A
ENST00000533133.6:c.1328+150G>A	ENSP00000433090.2:n.1328+150G>A
ENST00000533367.6:n.366+150G>A
ENST00000638487.1:c.*654+150G>A	ENSP00000492294.1:n.*654+150G>A
ENST00000638518.1:c.354-3966G>A
ENST00000638767.1:c.1889+150G>A	ENSP00000492220.1:n.1889+150G>A
ENST00000638790.1:c.1171+1329G>A	ENSP00000491457.1:n.1171+1329G>A
ENST00000639189.1:c.1143+1329G>A	ENSP00000491770.1:n.1143+1329G>A
ENST00000639457.1:c.*469+1329G>A	ENSP00000492391.1:n.*469+1329G>A
ENST00000639523.1:c.1263+150G>A
ENST00000639596.1:c.1143+1329G>A	ENSP00000491918.1:n.1143+1329G>A
ENST00000639724.1:c.1328+150G>A	ENSP00000492625.1:n.1328+150G>A
ENST00000640027.1:c.1328+150G>A	ENSP00000492872.1:n.1328+150G>A
ENST00000640077.1:c.1336+150G>A	ENSP00000490968.1:n.1336+150G>A
ENST00000640451.1:c.1175+150G>A	ENSP00000492530.1:n.1175+150G>A
ENST00000640473.1:c.*177+150G>A	ENSP00000491371.1:n.*177+150G>A
ENST00000640521.1:c.1328+150G>A	ENSP00000491108.1:n.1328+150G>A
ENST00000640583.1:n.1891+150G>A
ENST00000640804.1:n.1701+150G>A
ENST00000251871.7:c.1328+150G>A	ENSP00000251871.3:n.1328+150G>A
ENST00000531920.5:n.629+150G>A
ENST00000533133.5:c.*613+150G>A	ENSP00000433090.1:n.*613+150G>A
ENST00000533367.5:n.381+150G>A
NM_004268.4:c.1328+150G>A	NP_004259.3:n.1328+150G>A
XM_011543068.1:c.1328+150G>A	XP_011541370.1:n.1328+150G>A
XR_247218.1:n.1377+1329G>A
XR_947872.1:n.1562+150G>A
NM_004268.5:c.1328+150G>A MANE Select	NP_004259.3:n.1328+150G>A