Canonical Allele Identifier: CA2065410892

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970633C= , CM000674.2:g.115970633C=	GRCh38
NC_000012.11:g.116408438C= , CM000674.1:g.116408438C=	GRCh37
NC_000012.10:g.114892821C=	NCBI36
NG_023366.1:g.311554G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.6028G= MANE Select	ENSP00000281928.3:p.Ala2010=
ENST00000548784.2:n.2242G=
ENST00000648379.1:n.4396G=
ENST00000648737.1:n.5792G=
ENST00000648825.1:n.4213G=
ENST00000648916.1:n.4039G=
ENST00000649607.1:c.4212G=
ENST00000649775.1:c.2517G=
ENST00000650226.1:c.6064G=	ENSP00000496981.1:p.Ala2022=
ENST00000281928.7:c.6028G=	ENSP00000281928.3:p.Ala2010=
NM_015335.4:c.6028G=	NP_056150.1:p.Ala2010=
XM_011538080.1:c.6064G=	XP_011536382.1:p.Ala2022=
XM_011538081.1:c.6061G=	XP_011536383.1:p.Ala2021=
XM_011538082.1:c.6034G=	XP_011536384.1:p.Ala2012=
XM_011538080.2:c.6064G=	XP_011536382.1:p.Ala2022=
XM_011538081.2:c.6061G=	XP_011536383.1:p.Ala2021=
XM_011538082.2:c.6034G=	XP_011536384.1:p.Ala2012=
XM_017019090.1:c.6025G=	XP_016874579.1:p.Ala2009=
NM_015335.5:c.6028G= MANE Select	NP_056150.1:p.Ala2010=