Canonical Allele Identifier: CA2065412936

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975320A= , CM000674.2:g.115975320A=	GRCh38
NC_000012.11:g.116413125A= , CM000674.1:g.116413125A=	GRCh37
NC_000012.10:g.114897508A=	NCBI36
NG_023366.1:g.306867T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5589-7T= MANE Select	ENSP00000281928.3:n.5589-7T=
ENST00000548694.2:n.572T=
ENST00000648379.1:n.3957-7T=
ENST00000648737.1:n.5353-7T=
ENST00000648825.1:n.3774-7T=
ENST00000648916.1:n.3600-7T=
ENST00000649607.1:c.3773-7T=
ENST00000649775.1:c.2078-7T=
ENST00000650226.1:c.5618T=	ENSP00000496981.1:p.Phe1873=
ENST00000281928.7:c.5589-7T=	ENSP00000281928.3:n.5589-7T=
ENST00000548694.1:n.572T=
ENST00000552447.1:c.195T=
NM_015335.4:c.5589-7T=	NP_056150.1:n.5589-7T=
XM_011538080.1:c.5618T=	XP_011536382.1:p.Phe1873=
XM_011538081.1:c.5615T=	XP_011536383.1:p.Phe1872=
XM_011538082.1:c.5588T=	XP_011536384.1:p.Phe1863=
XM_011538080.2:c.5618T=	XP_011536382.1:p.Phe1873=
XM_011538081.2:c.5615T=	XP_011536383.1:p.Phe1872=
XM_011538082.2:c.5588T=	XP_011536384.1:p.Phe1863=
XM_017019090.1:c.5586-7T=	XP_016874579.1:n.5586-7T=
NM_015335.5:c.5589-7T= MANE Select	NP_056150.1:n.5589-7T=