Canonical Allele Identifier: CA2065359659

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975520T= , CM000674.2:g.115975520T=	GRCh38
NC_000012.11:g.116413325T= , CM000674.1:g.116413325T=	GRCh37
NC_000012.10:g.114897708T=	NCBI36
NG_023366.1:g.306667A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5583A= MANE Select	ENSP00000281928.3:p.Pro1861=
ENST00000548694.2:n.372A=
ENST00000648379.1:n.3951A=
ENST00000648737.1:n.5347A=
ENST00000648825.1:n.3768A=
ENST00000648916.1:n.3594A=
ENST00000649607.1:c.3767A=
ENST00000649775.1:c.2072A=
ENST00000650226.1:c.5583A=	ENSP00000496981.1:p.Pro1861=
ENST00000281928.7:c.5583A=	ENSP00000281928.3:p.Pro1861=
ENST00000548694.1:n.372A=
ENST00000552447.1:c.160A=
NM_015335.4:c.5583A=	NP_056150.1:p.Pro1861=
XM_011538080.1:c.5583A=	XP_011536382.1:p.Pro1861=
XM_011538081.1:c.5580A=	XP_011536383.1:p.Pro1860=
XM_011538082.1:c.5553A=	XP_011536384.1:p.Pro1851=
XM_011538080.2:c.5583A=	XP_011536382.1:p.Pro1861=
XM_011538081.2:c.5580A=	XP_011536383.1:p.Pro1860=
XM_011538082.2:c.5553A=	XP_011536384.1:p.Pro1851=
XM_017019090.1:c.5580A=	XP_016874579.1:p.Pro1860=
NM_015335.5:c.5583A= MANE Select	NP_056150.1:p.Pro1861=