Canonical Allele Identifier: CA2065504397

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116237681G= , CM000674.2:g.116237681G=	GRCh38
NC_000012.11:g.116675486G= , CM000674.1:g.116675486G=	GRCh37
NC_000012.10:g.115159869G=	NCBI36
NG_023366.1:g.44506C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.97C= MANE Select	ENSP00000281928.3:p.Arg33=
ENST00000548743.2:c.67C=	ENSP00000448553.2:p.Arg23=
ENST00000551197.2:c.47C=
ENST00000647567.1:c.7C=	ENSP00000497136.1:p.Arg3=
ENST00000650226.1:c.97C=	ENSP00000496981.1:p.Arg33=
ENST00000650375.1:n.259C=
ENST00000281928.7:c.97C=	ENSP00000281928.3:p.Arg33=
ENST00000548743.1:c.67C=	ENSP00000448553.1:p.Arg23=
ENST00000551197.1:n.47C=
NM_015335.4:c.97C=	NP_056150.1:p.Arg33=
XM_011538080.1:c.97C=	XP_011536382.1:p.Arg33=
XM_011538081.1:c.97C=	XP_011536383.1:p.Arg33=
XM_011538082.1:c.67C=	XP_011536384.1:p.Arg23=
XM_011538080.2:c.97C=	XP_011536382.1:p.Arg33=
XM_011538081.2:c.97C=	XP_011536383.1:p.Arg33=
XM_011538082.2:c.67C=	XP_011536384.1:p.Arg23=
XM_017019090.1:c.97C=	XP_016874579.1:p.Arg33=
NM_015335.5:c.97C= MANE Select	NP_056150.1:p.Arg33=