Canonical Allele Identifier: CA2065410936

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970763G= , CM000674.2:g.115970763G=	GRCh38
NC_000012.11:g.116408568G= , CM000674.1:g.116408568G=	GRCh37
NC_000012.10:g.114892951G=	NCBI36
NG_023366.1:g.311424C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5898C= MANE Select	ENSP00000281928.3:p.Val1966=
ENST00000548694.2:n.888C=
ENST00000548784.2:n.2112C=
ENST00000648379.1:n.4266C=
ENST00000648737.1:n.5662C=
ENST00000648825.1:n.4083C=
ENST00000648916.1:n.3909C=
ENST00000649607.1:c.4082C=
ENST00000649775.1:c.2387C=
ENST00000650226.1:c.5934C=	ENSP00000496981.1:p.Val1978=
ENST00000281928.7:c.5898C=	ENSP00000281928.3:p.Val1966=
ENST00000548784.1:n.396C=
ENST00000552447.1:c.511C=
NM_015335.4:c.5898C=	NP_056150.1:p.Val1966=
XM_011538080.1:c.5934C=	XP_011536382.1:p.Val1978=
XM_011538081.1:c.5931C=	XP_011536383.1:p.Val1977=
XM_011538082.1:c.5904C=	XP_011536384.1:p.Val1968=
XM_011538080.2:c.5934C=	XP_011536382.1:p.Val1978=
XM_011538081.2:c.5931C=	XP_011536383.1:p.Val1977=
XM_011538082.2:c.5904C=	XP_011536384.1:p.Val1968=
XM_017019090.1:c.5895C=	XP_016874579.1:p.Val1965=
NM_015335.5:c.5898C= MANE Select	NP_056150.1:p.Val1966=