Canonical Allele Identifier: CA2065371448

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982448A= , CM000674.2:g.115982448A=	GRCh38
NC_000012.11:g.116420253A= , CM000674.1:g.116420253A=	GRCh37
NC_000012.10:g.114904636A=	NCBI36
NG_023366.1:g.299739T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5111T= MANE Select	ENSP00000281928.3:p.Met1704=
ENST00000549786.2:c.4539T=
ENST00000648379.1:n.3479T=
ENST00000648737.1:n.4875T=
ENST00000648825.1:n.1851T=
ENST00000648916.1:n.3122T=
ENST00000649146.1:n.2354T=
ENST00000649607.1:c.3295T=
ENST00000649775.1:c.1600T=
ENST00000650226.1:c.5111T=	ENSP00000496981.1:p.Met1704=
ENST00000281928.7:c.5111T=	ENSP00000281928.3:p.Met1704=
ENST00000549786.1:c.475T=
ENST00000552340.1:c.143T=	ENSP00000449876.1:p.Met48=
NM_015335.4:c.5111T=	NP_056150.1:p.Met1704=
XM_011538080.1:c.5111T=	XP_011536382.1:p.Met1704=
XM_011538081.1:c.5108T=	XP_011536383.1:p.Met1703=
XM_011538082.1:c.5081T=	XP_011536384.1:p.Met1694=
XM_011538080.2:c.5111T=	XP_011536382.1:p.Met1704=
XM_011538081.2:c.5108T=	XP_011536383.1:p.Met1703=
XM_011538082.2:c.5081T=	XP_011536384.1:p.Met1694=
XM_017019090.1:c.5108T=	XP_016874579.1:p.Met1703=
NM_015335.5:c.5111T= MANE Select	NP_056150.1:p.Met1704=