Canonical Allele Identifier: CA2065359680

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975525A= , CM000674.2:g.115975525A=	GRCh38
NC_000012.11:g.116413330A= , CM000674.1:g.116413330A=	GRCh37
NC_000012.10:g.114897713A=	NCBI36
NG_023366.1:g.306662T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5578T= MANE Select	ENSP00000281928.3:p.Leu1860=
ENST00000548694.2:n.367T=
ENST00000648379.1:n.3946T=
ENST00000648737.1:n.5342T=
ENST00000648825.1:n.3763T=
ENST00000648916.1:n.3589T=
ENST00000649607.1:c.3762T=
ENST00000649775.1:c.2067T=
ENST00000650226.1:c.5578T=	ENSP00000496981.1:p.Leu1860=
ENST00000281928.7:c.5578T=	ENSP00000281928.3:p.Leu1860=
ENST00000548694.1:n.367T=
ENST00000552447.1:c.155T=
NM_015335.4:c.5578T=	NP_056150.1:p.Leu1860=
XM_011538080.1:c.5578T=	XP_011536382.1:p.Leu1860=
XM_011538081.1:c.5575T=	XP_011536383.1:p.Leu1859=
XM_011538082.1:c.5548T=	XP_011536384.1:p.Leu1850=
XM_011538080.2:c.5578T=	XP_011536382.1:p.Leu1860=
XM_011538081.2:c.5575T=	XP_011536383.1:p.Leu1859=
XM_011538082.2:c.5548T=	XP_011536384.1:p.Leu1850=
XM_017019090.1:c.5575T=	XP_016874579.1:p.Leu1859=
NM_015335.5:c.5578T= MANE Select	NP_056150.1:p.Leu1860=