Canonical Allele Identifier: CA2065410885

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970610C= , CM000674.2:g.115970610C=	GRCh38
NC_000012.11:g.116408415C= , CM000674.1:g.116408415C=	GRCh37
NC_000012.10:g.114892798C=	NCBI36
NG_023366.1:g.311577G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.6051G= MANE Select	ENSP00000281928.3:p.Gly2017=
ENST00000548784.2:n.2265G=
ENST00000648379.1:n.4419G=
ENST00000648737.1:n.5815G=
ENST00000648825.1:n.4236G=
ENST00000648916.1:n.4062G=
ENST00000649607.1:c.4235G=
ENST00000649775.1:c.2540G=
ENST00000650226.1:c.6087G=	ENSP00000496981.1:p.Gly2029=
ENST00000281928.7:c.6051G=	ENSP00000281928.3:p.Gly2017=
NM_015335.4:c.6051G=	NP_056150.1:p.Gly2017=
XM_011538080.1:c.6087G=	XP_011536382.1:p.Gly2029=
XM_011538081.1:c.6084G=	XP_011536383.1:p.Gly2028=
XM_011538082.1:c.6057G=	XP_011536384.1:p.Gly2019=
XM_011538080.2:c.6087G=	XP_011536382.1:p.Gly2029=
XM_011538081.2:c.6084G=	XP_011536383.1:p.Gly2028=
XM_011538082.2:c.6057G=	XP_011536384.1:p.Gly2019=
XM_017019090.1:c.6048G=	XP_016874579.1:p.Gly2016=
NM_015335.5:c.6051G= MANE Select	NP_056150.1:p.Gly2017=