Canonical Allele Identifier: CA2065371467

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982453G= , CM000674.2:g.115982453G=	GRCh38
NC_000012.11:g.116420258G= , CM000674.1:g.116420258G=	GRCh37
NC_000012.10:g.114904641G=	NCBI36
NG_023366.1:g.299734C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5106C= MANE Select	ENSP00000281928.3:p.Ser1702=
ENST00000549786.2:c.4534C=
ENST00000648379.1:n.3474C=
ENST00000648737.1:n.4870C=
ENST00000648825.1:n.1846C=
ENST00000648916.1:n.3117C=
ENST00000649146.1:n.2349C=
ENST00000649607.1:c.3290C=
ENST00000649775.1:c.1595C=
ENST00000650226.1:c.5106C=	ENSP00000496981.1:p.Ser1702=
ENST00000281928.7:c.5106C=	ENSP00000281928.3:p.Ser1702=
ENST00000549786.1:c.470C=
ENST00000552340.1:c.138C=	ENSP00000449876.1:p.Ser46=
NM_015335.4:c.5106C=	NP_056150.1:p.Ser1702=
XM_011538080.1:c.5106C=	XP_011536382.1:p.Ser1702=
XM_011538081.1:c.5103C=	XP_011536383.1:p.Ser1701=
XM_011538082.1:c.5076C=	XP_011536384.1:p.Ser1692=
XM_011538080.2:c.5106C=	XP_011536382.1:p.Ser1702=
XM_011538081.2:c.5103C=	XP_011536383.1:p.Ser1701=
XM_011538082.2:c.5076C=	XP_011536384.1:p.Ser1692=
XM_017019090.1:c.5103C=	XP_016874579.1:p.Ser1701=
NM_015335.5:c.5106C= MANE Select	NP_056150.1:p.Ser1702=