Canonical Allele Identifier: CA2065412937

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975322T= , CM000674.2:g.115975322T=	GRCh38
NC_000012.11:g.116413127T= , CM000674.1:g.116413127T=	GRCh37
NC_000012.10:g.114897510T=	NCBI36
NG_023366.1:g.306865A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5589-9A= MANE Select	ENSP00000281928.3:n.5589-9A=
ENST00000548694.2:n.570A=
ENST00000648379.1:n.3957-9A=
ENST00000648737.1:n.5353-9A=
ENST00000648825.1:n.3774-9A=
ENST00000648916.1:n.3600-9A=
ENST00000649607.1:c.3773-9A=
ENST00000649775.1:c.2078-9A=
ENST00000650226.1:c.5616A=	ENSP00000496981.1:p.Leu1872=
ENST00000281928.7:c.5589-9A=	ENSP00000281928.3:n.5589-9A=
ENST00000548694.1:n.570A=
ENST00000552447.1:c.193A=
NM_015335.4:c.5589-9A=	NP_056150.1:n.5589-9A=
XM_011538080.1:c.5616A=	XP_011536382.1:p.Leu1872=
XM_011538081.1:c.5613A=	XP_011536383.1:p.Leu1871=
XM_011538082.1:c.5586A=	XP_011536384.1:p.Leu1862=
XM_011538080.2:c.5616A=	XP_011536382.1:p.Leu1872=
XM_011538081.2:c.5613A=	XP_011536383.1:p.Leu1871=
XM_011538082.2:c.5586A=	XP_011536384.1:p.Leu1862=
XM_017019090.1:c.5586-9A=	XP_016874579.1:n.5586-9A=
NM_015335.5:c.5589-9A= MANE Select	NP_056150.1:n.5589-9A=