Canonical Allele Identifier: CA2065370822

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982155A= , CM000674.2:g.115982155A=	GRCh38
NC_000012.11:g.116419960A= , CM000674.1:g.116419960A=	GRCh37
NC_000012.10:g.114904343A=	NCBI36
NG_023366.1:g.300032T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5175+229T= MANE Select	ENSP00000281928.3:n.5175+229T=
ENST00000549786.2:c.4832T=
ENST00000648379.1:n.3543+229T=
ENST00000648737.1:n.4939+229T=
ENST00000648825.1:n.2144T=
ENST00000648916.1:n.3186+229T=
ENST00000649146.1:n.2647T=
ENST00000649607.1:c.3359+229T=
ENST00000649775.1:c.1664+229T=
ENST00000650226.1:c.5175+229T=	ENSP00000496981.1:n.5175+229T=
ENST00000281928.7:c.5175+229T=	ENSP00000281928.3:n.5175+229T=
ENST00000549786.1:c.768T=
ENST00000552340.1:c.207+229T=	ENSP00000449876.1:n.207+229T=
NM_015335.4:c.5175+229T=	NP_056150.1:n.5175+229T=
XM_011538080.1:c.5175+229T=	XP_011536382.1:n.5175+229T=
XM_011538081.1:c.5172+229T=	XP_011536383.1:n.5172+229T=
XM_011538082.1:c.5145+229T=	XP_011536384.1:n.5145+229T=
XM_011538080.2:c.5175+229T=	XP_011536382.1:n.5175+229T=
XM_011538081.2:c.5172+229T=	XP_011536383.1:n.5172+229T=
XM_011538082.2:c.5145+229T=	XP_011536384.1:n.5145+229T=
XM_017019090.1:c.5172+229T=	XP_016874579.1:n.5172+229T=
NM_015335.5:c.5175+229T= MANE Select	NP_056150.1:n.5175+229T=