Canonical Allele Identifier: CA2065375489

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984343G= , CM000674.2:g.115984343G=	GRCh38
NC_000012.11:g.116422148G= , CM000674.1:g.116422148G=	GRCh37
NC_000012.10:g.114906531G=	NCBI36
NG_023366.1:g.297844C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4368C= MANE Select	ENSP00000281928.3:p.Ile1456=
ENST00000549786.2:c.3796C=
ENST00000648379.1:n.2736C=
ENST00000648737.1:n.4132C=
ENST00000648825.1:n.1108C=
ENST00000648916.1:n.2379C=
ENST00000649146.1:n.1098C=
ENST00000649607.1:c.2552C=
ENST00000649775.1:c.865C=
ENST00000650091.1:n.2344C=
ENST00000650226.1:c.4368C=	ENSP00000496981.1:p.Ile1456=
ENST00000281928.7:c.4368C=	ENSP00000281928.3:p.Ile1456=
NM_015335.4:c.4368C=	NP_056150.1:p.Ile1456=
XM_011538080.1:c.4368C=	XP_011536382.1:p.Ile1456=
XM_011538081.1:c.4365C=	XP_011536383.1:p.Ile1455=
XM_011538082.1:c.4338C=	XP_011536384.1:p.Ile1446=
XM_011538080.2:c.4368C=	XP_011536382.1:p.Ile1456=
XM_011538081.2:c.4365C=	XP_011536383.1:p.Ile1455=
XM_011538082.2:c.4338C=	XP_011536384.1:p.Ile1446=
XM_017019090.1:c.4365C=	XP_016874579.1:p.Ile1455=
NM_015335.5:c.4368C= MANE Select	NP_056150.1:p.Ile1456=