Canonical Allele Identifier: CA226479558

Gene: MED17

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.93793425C>T , CM000673.2:g.93793425C>T	GRCh38
NC_000011.9:g.93526591C>T , CM000673.1:g.93526591C>T	GRCh37
NC_000011.8:g.93166239C>T	NCBI36
NG_028028.1:g.14187C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251871.9:c.638-303C>T MANE Select	ENSP00000251871.3:n.638-303C>T
ENST00000507258.4:n.726-303C>T
ENST00000525026.6:n.859-303C>T
ENST00000528786.2:c.411-303C>T	ENSP00000433626.2:n.411-303C>T
ENST00000529626.2:n.252C>T
ENST00000533133.6:c.638-303C>T	ENSP00000433090.2:n.638-303C>T
ENST00000638294.1:c.251-303C>T	ENSP00000491675.1:n.251-303C>T
ENST00000638487.1:c.638-303C>T	ENSP00000492294.1:n.638-303C>T
ENST00000638518.1:c.353+5258C>T
ENST00000638767.1:c.1199-303C>T	ENSP00000492220.1:n.1199-303C>T
ENST00000638790.1:c.476-303C>T	ENSP00000491457.1:n.476-303C>T
ENST00000639189.1:c.638-303C>T	ENSP00000491770.1:n.638-303C>T
ENST00000639457.1:c.638-303C>T	ENSP00000492391.1:n.638-303C>T
ENST00000639523.1:c.573-303C>T
ENST00000639596.1:c.638-303C>T	ENSP00000491918.1:n.638-303C>T
ENST00000639724.1:c.638-303C>T	ENSP00000492625.1:n.638-303C>T
ENST00000640027.1:c.638-303C>T	ENSP00000492872.1:n.638-303C>T
ENST00000640077.1:c.332-303C>T	ENSP00000490968.1:n.332-303C>T
ENST00000640451.1:c.638-303C>T	ENSP00000492530.1:n.638-303C>T
ENST00000640473.1:c.251-4110C>T	ENSP00000491371.1:n.251-4110C>T
ENST00000640521.1:c.638-303C>T	ENSP00000491108.1:n.638-303C>T
ENST00000640583.1:n.925-303C>T
ENST00000640804.1:n.925-303C>T
ENST00000251871.7:c.638-303C>T	ENSP00000251871.3:n.638-303C>T
ENST00000525026.5:n.2093-303C>T
ENST00000528786.1:c.314-303C>T	ENSP00000433626.1:n.314-303C>T
ENST00000533133.5:c.638-303C>T	ENSP00000433090.1:n.638-303C>T
NM_004268.4:c.638-303C>T	NP_004259.3:n.638-303C>T
XM_011543068.1:c.638-303C>T	XP_011541370.1:n.638-303C>T
XR_247218.1:n.872-303C>T
XR_947872.1:n.872-303C>T
NM_004268.5:c.638-303C>T MANE Select	NP_004259.3:n.638-303C>T