Canonical Allele Identifier: CA382357412

Gene: MED17

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.93796468T>G , CM000673.2:g.93796468T>G	GRCh38
NC_000011.9:g.93529634T>G , CM000673.1:g.93529634T>G	GRCh37
NC_000011.8:g.93169282T>G	NCBI36
NG_028028.1:g.17230T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004268.5:c.1071T>G MANE Select	NP_004259.3:p.Phe357Leu
ENST00000251871.9:c.1071T>G MANE Select	ENSP00000251871.3:p.Phe357Leu
NM_004268.4:c.1071T>G	NP_004259.3:p.Phe357Leu
ENST00000251871.7:c.1071T>G	ENSP00000251871.3:p.Phe357Leu
ENST00000507258.3:n.402T>G
ENST00000507258.4:n.2784T>G
ENST00000525026.5:n.2526T>G
ENST00000525026.6:n.1378T>G
ENST00000529626.2:n.1074T>G
ENST00000531920.5:n.372T>G
ENST00000531920.6:n.372T>G
ENST00000533133.5:c.*356T>G	ENSP00000433090.1:n.*356T>G
ENST00000533133.6:c.1071T>G	ENSP00000433090.2:p.Phe357Leu
ENST00000533367.5:n.124T>G
ENST00000533367.6:n.109T>G
ENST00000638487.1:c.*397T>G	ENSP00000492294.1:n.*397T>G
ENST00000638518.1:c.354-5367T>G
ENST00000638767.1:c.1632T>G	ENSP00000492220.1:p.Phe544Leu
ENST00000638790.1:c.1099T>G	ENSP00000491457.1:n.1099T>G
ENST00000639189.1:c.1071T>G	ENSP00000491770.1:p.Phe357Leu
ENST00000639457.1:c.*397T>G	ENSP00000492391.1:n.*397T>G
ENST00000639523.1:c.1006T>G
ENST00000639596.1:c.1071T>G	ENSP00000491918.1:p.Phe357Leu
ENST00000639724.1:c.1071T>G	ENSP00000492625.1:p.Phe357Leu
ENST00000640027.1:c.1071T>G	ENSP00000492872.1:p.Phe357Leu
ENST00000640077.1:c.554-469T>G	ENSP00000490968.1:n.554-469T>G
ENST00000640451.1:c.918T>G	ENSP00000492530.1:p.Phe306Leu
ENST00000640473.1:c.251-1067T>G	ENSP00000491371.1:n.251-1067T>G
ENST00000640521.1:c.1071T>G	ENSP00000491108.1:p.Phe357Leu
ENST00000640583.1:n.1634T>G
ENST00000640804.1:n.1444T>G
XM_011543068.1:c.1071T>G	XP_011541370.1:p.Phe357Leu
XR_247218.1:n.1305T>G
XR_947872.1:n.1305T>G