Canonical Allele Identifier: CA2065370887

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982206T= , CM000674.2:g.115982206T=	GRCh38
NC_000012.11:g.116420011T= , CM000674.1:g.116420011T=	GRCh37
NC_000012.10:g.114904394T=	NCBI36
NG_023366.1:g.299981A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5175+178A= MANE Select	ENSP00000281928.3:n.5175+178A=
ENST00000549786.2:c.4781A=
ENST00000648379.1:n.3543+178A=
ENST00000648737.1:n.4939+178A=
ENST00000648825.1:n.2093A=
ENST00000648916.1:n.3186+178A=
ENST00000649146.1:n.2596A=
ENST00000649607.1:c.3359+178A=
ENST00000649775.1:c.1664+178A=
ENST00000650226.1:c.5175+178A=	ENSP00000496981.1:n.5175+178A=
ENST00000281928.7:c.5175+178A=	ENSP00000281928.3:n.5175+178A=
ENST00000549786.1:c.717A=
ENST00000552340.1:c.207+178A=	ENSP00000449876.1:n.207+178A=
NM_015335.4:c.5175+178A=	NP_056150.1:n.5175+178A=
XM_011538080.1:c.5175+178A=	XP_011536382.1:n.5175+178A=
XM_011538081.1:c.5172+178A=	XP_011536383.1:n.5172+178A=
XM_011538082.1:c.5145+178A=	XP_011536384.1:n.5145+178A=
XM_011538080.2:c.5175+178A=	XP_011536382.1:n.5175+178A=
XM_011538081.2:c.5172+178A=	XP_011536383.1:n.5172+178A=
XM_011538082.2:c.5145+178A=	XP_011536384.1:n.5145+178A=
XM_017019090.1:c.5172+178A=	XP_016874579.1:n.5172+178A=
NM_015335.5:c.5175+178A= MANE Select	NP_056150.1:n.5175+178A=