Canonical Allele Identifier: CA2065371502

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982471C= , CM000674.2:g.115982471C=	GRCh38
NC_000012.11:g.116420276C= , CM000674.1:g.116420276C=	GRCh37
NC_000012.10:g.114904659C=	NCBI36
NG_023366.1:g.299716G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5088G= MANE Select	ENSP00000281928.3:p.Gly1696=
ENST00000549786.2:c.4516G=
ENST00000648379.1:n.3456G=
ENST00000648737.1:n.4852G=
ENST00000648825.1:n.1828G=
ENST00000648916.1:n.3099G=
ENST00000649146.1:n.2331G=
ENST00000649607.1:c.3272G=
ENST00000649775.1:c.1577G=
ENST00000650226.1:c.5088G=	ENSP00000496981.1:p.Gly1696=
ENST00000281928.7:c.5088G=	ENSP00000281928.3:p.Gly1696=
ENST00000549786.1:c.452G=
ENST00000552340.1:c.120G=	ENSP00000449876.1:p.Gly40=
NM_015335.4:c.5088G=	NP_056150.1:p.Gly1696=
XM_011538080.1:c.5088G=	XP_011536382.1:p.Gly1696=
XM_011538081.1:c.5085G=	XP_011536383.1:p.Gly1695=
XM_011538082.1:c.5058G=	XP_011536384.1:p.Gly1686=
XM_011538080.2:c.5088G=	XP_011536382.1:p.Gly1696=
XM_011538081.2:c.5085G=	XP_011536383.1:p.Gly1695=
XM_011538082.2:c.5058G=	XP_011536384.1:p.Gly1686=
XM_017019090.1:c.5085G=	XP_016874579.1:p.Gly1695=
NM_015335.5:c.5088G= MANE Select	NP_056150.1:p.Gly1696=