Canonical Allele Identifier: CA2697548877

Gene: MED17

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.93787984T>G , CM000673.2:g.93787984T>G	GRCh38
NC_000011.9:g.93521150T>G , CM000673.1:g.93521150T>G	GRCh37
NC_000011.8:g.93160798T>G	NCBI36
NG_028028.1:g.8746T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251871.9:c.251-17T>G MANE Select	ENSP00000251871.3:n.251-17T>G
ENST00000507258.4:n.339-17T>G
ENST00000525026.6:n.472-17T>G
ENST00000528786.2:c.191-2590T>G	ENSP00000433626.2:n.191-2590T>G
ENST00000533133.6:c.251-17T>G	ENSP00000433090.2:n.251-17T>G
ENST00000638294.1:c.250+3221T>G	ENSP00000491675.1:n.250+3221T>G
ENST00000638487.1:c.251-17T>G	ENSP00000492294.1:n.251-17T>G
ENST00000638518.1:c.187-17T>G
ENST00000638767.1:c.812-17T>G	ENSP00000492220.1:n.812-17T>G
ENST00000638790.1:c.89-17T>G	ENSP00000491457.1:n.89-17T>G
ENST00000639189.1:c.251-17T>G	ENSP00000491770.1:n.251-17T>G
ENST00000639457.1:c.251-17T>G	ENSP00000492391.1:n.251-17T>G
ENST00000639523.1:c.186-17T>G
ENST00000639596.1:c.251-17T>G	ENSP00000491918.1:n.251-17T>G
ENST00000639724.1:c.251-17T>G	ENSP00000492625.1:n.251-17T>G
ENST00000640027.1:c.251-17T>G	ENSP00000492872.1:n.251-17T>G
ENST00000640451.1:c.251-17T>G	ENSP00000492530.1:n.251-17T>G
ENST00000640473.1:c.250+3221T>G	ENSP00000491371.1:n.250+3221T>G
ENST00000640521.1:c.251-17T>G	ENSP00000491108.1:n.251-17T>G
ENST00000640583.1:n.538-17T>G
ENST00000640804.1:n.538-17T>G
ENST00000251871.7:c.251-17T>G	ENSP00000251871.3:n.251-17T>G
ENST00000528786.1:c.-74-17T>G	ENSP00000433626.1:n.-74-17T>G
ENST00000530819.1:c.251-17T>G	ENSP00000434459.1:n.251-17T>G
ENST00000533133.5:c.251-17T>G	ENSP00000433090.1:n.251-17T>G
ENST00000533359.5:c.251-17T>G	ENSP00000431524.1:n.251-17T>G
NM_004268.4:c.251-17T>G	NP_004259.3:n.251-17T>G
XM_011543068.1:c.251-17T>G	XP_011541370.1:n.251-17T>G
XR_247218.1:n.485-17T>G
XR_947872.1:n.485-17T>G
NM_004268.5:c.251-17T>G MANE Select	NP_004259.3:n.251-17T>G