Canonical Allele Identifier: CA2065371377

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982425C= , CM000674.2:g.115982425C=	GRCh38
NC_000012.11:g.116420230C= , CM000674.1:g.116420230C=	GRCh37
NC_000012.10:g.114904613C=	NCBI36
NG_023366.1:g.299762G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5134G= MANE Select	ENSP00000281928.3:p.Asp1712=
ENST00000549786.2:c.4562G=
ENST00000648379.1:n.3502G=
ENST00000648737.1:n.4898G=
ENST00000648825.1:n.1874G=
ENST00000648916.1:n.3145G=
ENST00000649146.1:n.2377G=
ENST00000649607.1:c.3318G=
ENST00000649775.1:c.1623G=
ENST00000650226.1:c.5134G=	ENSP00000496981.1:p.Asp1712=
ENST00000281928.7:c.5134G=	ENSP00000281928.3:p.Asp1712=
ENST00000549786.1:c.498G=
ENST00000552340.1:c.166G=	ENSP00000449876.1:p.Asp56=
NM_015335.4:c.5134G=	NP_056150.1:p.Asp1712=
XM_011538080.1:c.5134G=	XP_011536382.1:p.Asp1712=
XM_011538081.1:c.5131G=	XP_011536383.1:p.Asp1711=
XM_011538082.1:c.5104G=	XP_011536384.1:p.Asp1702=
XM_011538080.2:c.5134G=	XP_011536382.1:p.Asp1712=
XM_011538081.2:c.5131G=	XP_011536383.1:p.Asp1711=
XM_011538082.2:c.5104G=	XP_011536384.1:p.Asp1702=
XM_017019090.1:c.5131G=	XP_016874579.1:p.Asp1711=
NM_015335.5:c.5134G= MANE Select	NP_056150.1:p.Asp1712=