Canonical Allele Identifier: CA2065371106

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982335A= , CM000674.2:g.115982335A=	GRCh38
NC_000012.11:g.116420140A= , CM000674.1:g.116420140A=	GRCh37
NC_000012.10:g.114904523A=	NCBI36
NG_023366.1:g.299852T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5175+49T= MANE Select	ENSP00000281928.3:n.5175+49T=
ENST00000549786.2:c.4652T=
ENST00000648379.1:n.3543+49T=
ENST00000648737.1:n.4939+49T=
ENST00000648825.1:n.1964T=
ENST00000648916.1:n.3186+49T=
ENST00000649146.1:n.2467T=
ENST00000649607.1:c.3359+49T=
ENST00000649775.1:c.1664+49T=
ENST00000650226.1:c.5175+49T=	ENSP00000496981.1:n.5175+49T=
ENST00000281928.7:c.5175+49T=	ENSP00000281928.3:n.5175+49T=
ENST00000549786.1:c.588T=
ENST00000552340.1:c.207+49T=	ENSP00000449876.1:n.207+49T=
NM_015335.4:c.5175+49T=	NP_056150.1:n.5175+49T=
XM_011538080.1:c.5175+49T=	XP_011536382.1:n.5175+49T=
XM_011538081.1:c.5172+49T=	XP_011536383.1:n.5172+49T=
XM_011538082.1:c.5145+49T=	XP_011536384.1:n.5145+49T=
XM_011538080.2:c.5175+49T=	XP_011536382.1:n.5175+49T=
XM_011538081.2:c.5172+49T=	XP_011536383.1:n.5172+49T=
XM_011538082.2:c.5145+49T=	XP_011536384.1:n.5145+49T=
XM_017019090.1:c.5172+49T=	XP_016874579.1:n.5172+49T=
NM_015335.5:c.5175+49T= MANE Select	NP_056150.1:n.5175+49T=