Canonical Allele Identifier: CA2065371721

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982551T= , CM000674.2:g.115982551T=	GRCh38
NC_000012.11:g.116420356T= , CM000674.1:g.116420356T=	GRCh37
NC_000012.10:g.114904739T=	NCBI36
NG_023366.1:g.299636A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5008A= MANE Select	ENSP00000281928.3:p.Ser1670=
ENST00000549786.2:c.4436A=
ENST00000648379.1:n.3376A=
ENST00000648737.1:n.4772A=
ENST00000648825.1:n.1748A=
ENST00000648916.1:n.3019A=
ENST00000649146.1:n.2251A=
ENST00000649607.1:c.3192A=
ENST00000649775.1:c.1497A=
ENST00000650226.1:c.5008A=	ENSP00000496981.1:p.Ser1670=
ENST00000281928.7:c.5008A=	ENSP00000281928.3:p.Ser1670=
ENST00000549786.1:c.372A=
ENST00000552340.1:c.40A=	ENSP00000449876.1:p.Ser14=
NM_015335.4:c.5008A=	NP_056150.1:p.Ser1670=
XM_011538080.1:c.5008A=	XP_011536382.1:p.Ser1670=
XM_011538081.1:c.5005A=	XP_011536383.1:p.Ser1669=
XM_011538082.1:c.4978A=	XP_011536384.1:p.Ser1660=
XM_011538080.2:c.5008A=	XP_011536382.1:p.Ser1670=
XM_011538081.2:c.5005A=	XP_011536383.1:p.Ser1669=
XM_011538082.2:c.4978A=	XP_011536384.1:p.Ser1660=
XM_017019090.1:c.5005A=	XP_016874579.1:p.Ser1669=
NM_015335.5:c.5008A= MANE Select	NP_056150.1:p.Ser1670=