Canonical Allele Identifier: CA2065398801

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116022578G= , CM000674.2:g.116022578G=	GRCh38
NC_000012.11:g.116460383G= , CM000674.1:g.116460383G=	GRCh37
NC_000012.10:g.114944766G=	NCBI36
NG_023366.1:g.259609C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.503C= MANE Select	ENSP00000281928.3:p.Thr168=
ENST00000548743.2:c.473C=	ENSP00000448553.2:p.Thr158=
ENST00000647567.1:c.413C=	ENSP00000497136.1:p.Thr138=
ENST00000648737.1:n.267C=
ENST00000650226.1:c.503C=	ENSP00000496981.1:p.Thr168=
ENST00000281928.7:c.503C=	ENSP00000281928.3:p.Thr168=
NM_015335.4:c.503C=	NP_056150.1:p.Thr168=
XM_011538080.1:c.503C=	XP_011536382.1:p.Thr168=
XM_011538081.1:c.503C=	XP_011536383.1:p.Thr168=
XM_011538082.1:c.473C=	XP_011536384.1:p.Thr158=
XM_011538080.2:c.503C=	XP_011536382.1:p.Thr168=
XM_011538081.2:c.503C=	XP_011536383.1:p.Thr168=
XM_011538082.2:c.473C=	XP_011536384.1:p.Thr158=
XM_017019090.1:c.503C=	XP_016874579.1:p.Thr168=
NM_015335.5:c.503C= MANE Select	NP_056150.1:p.Thr168=