Canonical Allele Identifier: CA476484158

Gene: MED17

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.93784528C>G , CM000673.2:g.93784528C>G	GRCh38
NC_000011.9:g.93517694C>G , CM000673.1:g.93517694C>G	GRCh37
NC_000011.8:g.93157342C>G	NCBI36
NG_028028.1:g.5290C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251871.9:c.15C>G MANE Select	ENSP00000251871.3:p.Arg5=
ENST00000507258.4:n.103C>G
ENST00000525026.6:n.236C>G
ENST00000533133.6:c.15C>G	ENSP00000433090.2:p.Arg5=
ENST00000638294.1:c.15C>G	ENSP00000491675.1:p.Arg5=
ENST00000638487.1:c.15C>G	ENSP00000492294.1:p.Arg5=
ENST00000638767.1:c.676-100C>G	ENSP00000492220.1:n.676-100C>G
ENST00000639189.1:c.15C>G	ENSP00000491770.1:p.Arg5=
ENST00000639457.1:c.15C>G	ENSP00000492391.1:p.Arg5=
ENST00000639596.1:c.15C>G	ENSP00000491918.1:p.Arg5=
ENST00000639724.1:c.15C>G	ENSP00000492625.1:p.Arg5=
ENST00000640027.1:c.15C>G	ENSP00000492872.1:p.Arg5=
ENST00000640451.1:c.15C>G	ENSP00000492530.1:p.Arg5=
ENST00000640473.1:c.15C>G	ENSP00000491371.1:p.Arg5=
ENST00000640521.1:c.15C>G	ENSP00000491108.1:p.Arg5=
ENST00000640583.1:n.302C>G
ENST00000640804.1:n.302C>G
ENST00000251871.7:c.15C>G	ENSP00000251871.3:p.Arg5=
ENST00000530819.1:c.15C>G	ENSP00000434459.1:p.Arg5=
ENST00000533133.5:c.15C>G	ENSP00000433090.1:p.Arg5=
ENST00000533359.5:c.15C>G	ENSP00000431524.1:p.Arg5=
NM_004268.4:c.15C>G	NP_004259.3:p.Arg5=
XM_011543068.1:c.15C>G	XP_011541370.1:p.Arg5=
XR_247218.1:n.249C>G
XR_947872.1:n.249C>G
NM_004268.5:c.15C>G MANE Select	NP_004259.3:p.Arg5=