Canonical Allele Identifier: CA476484521

Gene: MED17

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.93784711C>T , CM000673.2:g.93784711C>T	GRCh38
NC_000011.9:g.93517877C>T , CM000673.1:g.93517877C>T	GRCh37
NC_000011.8:g.93157525C>T	NCBI36
NG_028028.1:g.5473C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251871.9:c.198C>T MANE Select	ENSP00000251871.3:p.Asp66=
ENST00000507258.4:n.286C>T
ENST00000525026.6:n.419C>T
ENST00000528786.2:c.138C>T	ENSP00000433626.2:p.Asp46=
ENST00000533133.6:c.198C>T	ENSP00000433090.2:p.Asp66=
ENST00000638294.1:c.198C>T	ENSP00000491675.1:p.Asp66=
ENST00000638487.1:c.198C>T	ENSP00000492294.1:p.Asp66=
ENST00000638518.1:c.134C>T
ENST00000638767.1:c.759C>T	ENSP00000492220.1:p.Asp253=
ENST00000638790.1:c.36C>T	ENSP00000491457.1:p.Asp12=
ENST00000639189.1:c.198C>T	ENSP00000491770.1:p.Asp66=
ENST00000639457.1:c.198C>T	ENSP00000492391.1:p.Asp66=
ENST00000639596.1:c.198C>T	ENSP00000491918.1:p.Asp66=
ENST00000639724.1:c.198C>T	ENSP00000492625.1:p.Asp66=
ENST00000640027.1:c.198C>T	ENSP00000492872.1:p.Asp66=
ENST00000640451.1:c.198C>T	ENSP00000492530.1:p.Asp66=
ENST00000640473.1:c.198C>T	ENSP00000491371.1:p.Asp66=
ENST00000640521.1:c.198C>T	ENSP00000491108.1:p.Asp66=
ENST00000640583.1:n.485C>T
ENST00000640804.1:n.485C>T
ENST00000251871.7:c.198C>T	ENSP00000251871.3:p.Asp66=
ENST00000530819.1:c.198C>T	ENSP00000434459.1:p.Asp66=
ENST00000533133.5:c.198C>T	ENSP00000433090.1:p.Asp66=
ENST00000533359.5:c.198C>T	ENSP00000431524.1:p.Asp66=
NM_004268.4:c.198C>T	NP_004259.3:p.Asp66=
XM_011543068.1:c.198C>T	XP_011541370.1:p.Asp66=
XR_247218.1:n.432C>T
XR_947872.1:n.432C>T
NM_004268.5:c.198C>T MANE Select	NP_004259.3:p.Asp66=