Canonical Allele Identifier: CA2065412930

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975308C= , CM000674.2:g.115975308C=	GRCh38
NC_000012.11:g.116413113C= , CM000674.1:g.116413113C=	GRCh37
NC_000012.10:g.114897496C=	NCBI36
NG_023366.1:g.306879G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5594G= MANE Select	ENSP00000281928.3:p.Arg1865=
ENST00000548694.2:n.584G=
ENST00000648379.1:n.3962G=
ENST00000648737.1:n.5358G=
ENST00000648825.1:n.3779G=
ENST00000648916.1:n.3605G=
ENST00000649607.1:c.3778G=
ENST00000649775.1:c.2083G=
ENST00000650226.1:c.5630G=	ENSP00000496981.1:p.Arg1877=
ENST00000281928.7:c.5594G=	ENSP00000281928.3:p.Arg1865=
ENST00000548694.1:n.584G=
ENST00000552447.1:c.207G=
NM_015335.4:c.5594G=	NP_056150.1:p.Arg1865=
XM_011538080.1:c.5630G=	XP_011536382.1:p.Arg1877=
XM_011538081.1:c.5627G=	XP_011536383.1:p.Arg1876=
XM_011538082.1:c.5600G=	XP_011536384.1:p.Arg1867=
XM_011538080.2:c.5630G=	XP_011536382.1:p.Arg1877=
XM_011538081.2:c.5627G=	XP_011536383.1:p.Arg1876=
XM_011538082.2:c.5600G=	XP_011536384.1:p.Arg1867=
XM_017019090.1:c.5591G=	XP_016874579.1:p.Arg1864=
NM_015335.5:c.5594G= MANE Select	NP_056150.1:p.Arg1865=