Canonical Allele Identifier: CA2065412982

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975410A= , CM000674.2:g.115975410A=	GRCh38
NC_000012.11:g.116413215A= , CM000674.1:g.116413215A=	GRCh37
NC_000012.10:g.114897598A=	NCBI36
NG_023366.1:g.306777T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5589-97T= MANE Select	ENSP00000281928.3:n.5589-97T=
ENST00000548694.2:n.482T=
ENST00000648379.1:n.3957-97T=
ENST00000648737.1:n.5353-97T=
ENST00000648825.1:n.3774-97T=
ENST00000648916.1:n.3600-97T=
ENST00000649607.1:c.3773-97T=
ENST00000649775.1:c.2078-97T=
ENST00000650226.1:c.5589-61T=	ENSP00000496981.1:n.5589-61T=
ENST00000281928.7:c.5589-97T=	ENSP00000281928.3:n.5589-97T=
ENST00000548694.1:n.482T=
ENST00000552447.1:c.166-61T=
NM_015335.4:c.5589-97T=	NP_056150.1:n.5589-97T=
XM_011538080.1:c.5589-61T=	XP_011536382.1:n.5589-61T=
XM_011538081.1:c.5586-61T=	XP_011536383.1:n.5586-61T=
XM_011538082.1:c.5559-61T=	XP_011536384.1:n.5559-61T=
XM_011538080.2:c.5589-61T=	XP_011536382.1:n.5589-61T=
XM_011538081.2:c.5586-61T=	XP_011536383.1:n.5586-61T=
XM_011538082.2:c.5559-61T=	XP_011536384.1:n.5559-61T=
XM_017019090.1:c.5586-97T=	XP_016874579.1:n.5586-97T=
NM_015335.5:c.5589-97T= MANE Select	NP_056150.1:n.5589-97T=