Canonical Allele Identifier: CA2065359688

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975530A= , CM000674.2:g.115975530A=	GRCh38
NC_000012.11:g.116413335A= , CM000674.1:g.116413335A=	GRCh37
NC_000012.10:g.114897718A=	NCBI36
NG_023366.1:g.306657T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5573T= MANE Select	ENSP00000281928.3:p.Ile1858=
ENST00000548694.2:n.362T=
ENST00000648379.1:n.3941T=
ENST00000648737.1:n.5337T=
ENST00000648825.1:n.3758T=
ENST00000648916.1:n.3584T=
ENST00000649607.1:c.3757T=
ENST00000649775.1:c.2062T=
ENST00000650226.1:c.5573T=	ENSP00000496981.1:p.Ile1858=
ENST00000281928.7:c.5573T=	ENSP00000281928.3:p.Ile1858=
ENST00000548694.1:n.362T=
ENST00000552447.1:c.150T=
NM_015335.4:c.5573T=	NP_056150.1:p.Ile1858=
XM_011538080.1:c.5573T=	XP_011536382.1:p.Ile1858=
XM_011538081.1:c.5570T=	XP_011536383.1:p.Ile1857=
XM_011538082.1:c.5543T=	XP_011536384.1:p.Ile1848=
XM_011538080.2:c.5573T=	XP_011536382.1:p.Ile1858=
XM_011538081.2:c.5570T=	XP_011536383.1:p.Ile1857=
XM_011538082.2:c.5543T=	XP_011536384.1:p.Ile1848=
XM_017019090.1:c.5570T=	XP_016874579.1:p.Ile1857=
NM_015335.5:c.5573T= MANE Select	NP_056150.1:p.Ile1858=