Canonical Allele Identifier: CA2065371583

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982496G= , CM000674.2:g.115982496G=	GRCh38
NC_000012.11:g.116420301G= , CM000674.1:g.116420301G=	GRCh37
NC_000012.10:g.114904684G=	NCBI36
NG_023366.1:g.299691C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5063C= MANE Select	ENSP00000281928.3:p.Ala1688=
ENST00000549786.2:c.4491C=
ENST00000648379.1:n.3431C=
ENST00000648737.1:n.4827C=
ENST00000648825.1:n.1803C=
ENST00000648916.1:n.3074C=
ENST00000649146.1:n.2306C=
ENST00000649607.1:c.3247C=
ENST00000649775.1:c.1552C=
ENST00000650226.1:c.5063C=	ENSP00000496981.1:p.Ala1688=
ENST00000281928.7:c.5063C=	ENSP00000281928.3:p.Ala1688=
ENST00000549786.1:c.427C=
ENST00000552340.1:c.95C=	ENSP00000449876.1:p.Ala32=
NM_015335.4:c.5063C=	NP_056150.1:p.Ala1688=
XM_011538080.1:c.5063C=	XP_011536382.1:p.Ala1688=
XM_011538081.1:c.5060C=	XP_011536383.1:p.Ala1687=
XM_011538082.1:c.5033C=	XP_011536384.1:p.Ala1678=
XM_011538080.2:c.5063C=	XP_011536382.1:p.Ala1688=
XM_011538081.2:c.5060C=	XP_011536383.1:p.Ala1687=
XM_011538082.2:c.5033C=	XP_011536384.1:p.Ala1678=
XM_017019090.1:c.5060C=	XP_016874579.1:p.Ala1687=
NM_015335.5:c.5063C= MANE Select	NP_056150.1:p.Ala1688=