Canonical Allele Identifier: CA2065371505

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982473C= , CM000674.2:g.115982473C=	GRCh38
NC_000012.11:g.116420278C= , CM000674.1:g.116420278C=	GRCh37
NC_000012.10:g.114904661C=	NCBI36
NG_023366.1:g.299714G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5086G= MANE Select	ENSP00000281928.3:p.Gly1696=
ENST00000549786.2:c.4514G=
ENST00000648379.1:n.3454G=
ENST00000648737.1:n.4850G=
ENST00000648825.1:n.1826G=
ENST00000648916.1:n.3097G=
ENST00000649146.1:n.2329G=
ENST00000649607.1:c.3270G=
ENST00000649775.1:c.1575G=
ENST00000650226.1:c.5086G=	ENSP00000496981.1:p.Gly1696=
ENST00000281928.7:c.5086G=	ENSP00000281928.3:p.Gly1696=
ENST00000549786.1:c.450G=
ENST00000552340.1:c.118G=	ENSP00000449876.1:p.Gly40=
NM_015335.4:c.5086G=	NP_056150.1:p.Gly1696=
XM_011538080.1:c.5086G=	XP_011536382.1:p.Gly1696=
XM_011538081.1:c.5083G=	XP_011536383.1:p.Gly1695=
XM_011538082.1:c.5056G=	XP_011536384.1:p.Gly1686=
XM_011538080.2:c.5086G=	XP_011536382.1:p.Gly1696=
XM_011538081.2:c.5083G=	XP_011536383.1:p.Gly1695=
XM_011538082.2:c.5056G=	XP_011536384.1:p.Gly1686=
XM_017019090.1:c.5083G=	XP_016874579.1:p.Gly1695=
NM_015335.5:c.5086G= MANE Select	NP_056150.1:p.Gly1696=