Canonical Allele Identifier: CA2065410896

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970646G= , CM000674.2:g.115970646G=	GRCh38
NC_000012.11:g.116408451G= , CM000674.1:g.116408451G=	GRCh37
NC_000012.10:g.114892834G=	NCBI36
NG_023366.1:g.311541C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.6015C= MANE Select	ENSP00000281928.3:p.Ile2005=
ENST00000548784.2:n.2229C=
ENST00000648379.1:n.4383C=
ENST00000648737.1:n.5779C=
ENST00000648825.1:n.4200C=
ENST00000648916.1:n.4026C=
ENST00000649607.1:c.4199C=
ENST00000649775.1:c.2504C=
ENST00000650226.1:c.6051C=	ENSP00000496981.1:p.Ile2017=
ENST00000281928.7:c.6015C=	ENSP00000281928.3:p.Ile2005=
NM_015335.4:c.6015C=	NP_056150.1:p.Ile2005=
XM_011538080.1:c.6051C=	XP_011536382.1:p.Ile2017=
XM_011538081.1:c.6048C=	XP_011536383.1:p.Ile2016=
XM_011538082.1:c.6021C=	XP_011536384.1:p.Ile2007=
XM_011538080.2:c.6051C=	XP_011536382.1:p.Ile2017=
XM_011538081.2:c.6048C=	XP_011536383.1:p.Ile2016=
XM_011538082.2:c.6021C=	XP_011536384.1:p.Ile2007=
XM_017019090.1:c.6012C=	XP_016874579.1:p.Ile2004=
NM_015335.5:c.6015C= MANE Select	NP_056150.1:p.Ile2005=