Canonical Allele Identifier: CA2065410905

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970673G= , CM000674.2:g.115970673G=	GRCh38
NC_000012.11:g.116408478G= , CM000674.1:g.116408478G=	GRCh37
NC_000012.10:g.114892861G=	NCBI36
NG_023366.1:g.311514C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5988C= MANE Select	ENSP00000281928.3:p.Ile1996=
ENST00000548784.2:n.2202C=
ENST00000648379.1:n.4356C=
ENST00000648737.1:n.5752C=
ENST00000648825.1:n.4173C=
ENST00000648916.1:n.3999C=
ENST00000649607.1:c.4172C=
ENST00000649775.1:c.2477C=
ENST00000650226.1:c.6024C=	ENSP00000496981.1:p.Ile2008=
ENST00000281928.7:c.5988C=	ENSP00000281928.3:p.Ile1996=
NM_015335.4:c.5988C=	NP_056150.1:p.Ile1996=
XM_011538080.1:c.6024C=	XP_011536382.1:p.Ile2008=
XM_011538081.1:c.6021C=	XP_011536383.1:p.Ile2007=
XM_011538082.1:c.5994C=	XP_011536384.1:p.Ile1998=
XM_011538080.2:c.6024C=	XP_011536382.1:p.Ile2008=
XM_011538081.2:c.6021C=	XP_011536383.1:p.Ile2007=
XM_011538082.2:c.5994C=	XP_011536384.1:p.Ile1998=
XM_017019090.1:c.5985C=	XP_016874579.1:p.Ile1995=
NM_015335.5:c.5988C= MANE Select	NP_056150.1:p.Ile1996=