Canonical Allele Identifier: CA2065371819

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982579T= , CM000674.2:g.115982579T=	GRCh38
NC_000012.11:g.116420384T= , CM000674.1:g.116420384T=	GRCh37
NC_000012.10:g.114904767T=	NCBI36
NG_023366.1:g.299608A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4980A= MANE Select	ENSP00000281928.3:p.Gly1660=
ENST00000549786.2:c.4408A=
ENST00000648379.1:n.3348A=
ENST00000648737.1:n.4744A=
ENST00000648825.1:n.1720A=
ENST00000648916.1:n.2991A=
ENST00000649146.1:n.2223A=
ENST00000649607.1:c.3164A=
ENST00000649775.1:c.1469A=
ENST00000650226.1:c.4980A=	ENSP00000496981.1:p.Gly1660=
ENST00000281928.7:c.4980A=	ENSP00000281928.3:p.Gly1660=
ENST00000549786.1:c.344A=
ENST00000552340.1:c.12A=	ENSP00000449876.1:p.Gly4=
NM_015335.4:c.4980A=	NP_056150.1:p.Gly1660=
XM_011538080.1:c.4980A=	XP_011536382.1:p.Gly1660=
XM_011538081.1:c.4977A=	XP_011536383.1:p.Gly1659=
XM_011538082.1:c.4950A=	XP_011536384.1:p.Gly1650=
XM_011538080.2:c.4980A=	XP_011536382.1:p.Gly1660=
XM_011538081.2:c.4977A=	XP_011536383.1:p.Gly1659=
XM_011538082.2:c.4950A=	XP_011536384.1:p.Gly1650=
XM_017019090.1:c.4977A=	XP_016874579.1:p.Gly1659=
NM_015335.5:c.4980A= MANE Select	NP_056150.1:p.Gly1660=