Canonical Allele Identifier: CA2065410918

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970711G= , CM000674.2:g.115970711G=	GRCh38
NC_000012.11:g.116408516G= , CM000674.1:g.116408516G=	GRCh37
NC_000012.10:g.114892899G=	NCBI36
NG_023366.1:g.311476C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.5950C= MANE Select	ENSP00000281928.3:p.Gln1984=
ENST00000548784.2:n.2164C=
ENST00000648379.1:n.4318C=
ENST00000648737.1:n.5714C=
ENST00000648825.1:n.4135C=
ENST00000648916.1:n.3961C=
ENST00000649607.1:c.4134C=
ENST00000649775.1:c.2439C=
ENST00000650226.1:c.5986C=	ENSP00000496981.1:p.Gln1996=
ENST00000281928.7:c.5950C=	ENSP00000281928.3:p.Gln1984=
ENST00000548784.1:n.448C=
ENST00000552447.1:c.563C=
NM_015335.4:c.5950C=	NP_056150.1:p.Gln1984=
XM_011538080.1:c.5986C=	XP_011536382.1:p.Gln1996=
XM_011538081.1:c.5983C=	XP_011536383.1:p.Gln1995=
XM_011538082.1:c.5956C=	XP_011536384.1:p.Gln1986=
XM_011538080.2:c.5986C=	XP_011536382.1:p.Gln1996=
XM_011538081.2:c.5983C=	XP_011536383.1:p.Gln1995=
XM_011538082.2:c.5956C=	XP_011536384.1:p.Gln1986=
XM_017019090.1:c.5947C=	XP_016874579.1:p.Gln1983=
NM_015335.5:c.5950C= MANE Select	NP_056150.1:p.Gln1984=