Canonical Allele Identifier: CA2065410933

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970759T= , CM000674.2:g.115970759T=	GRCh38
NC_000012.11:g.116408564T= , CM000674.1:g.116408564T=	GRCh37
NC_000012.10:g.114892947T=	NCBI36
NG_023366.1:g.311428A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5902A= MANE Select	ENSP00000281928.3:p.Met1968=
ENST00000548784.2:n.2116A=
ENST00000648379.1:n.4270A=
ENST00000648737.1:n.5666A=
ENST00000648825.1:n.4087A=
ENST00000648916.1:n.3913A=
ENST00000649607.1:c.4086A=
ENST00000649775.1:c.2391A=
ENST00000650226.1:c.5938A=	ENSP00000496981.1:p.Met1980=
ENST00000281928.7:c.5902A=	ENSP00000281928.3:p.Met1968=
ENST00000548784.1:n.400A=
ENST00000552447.1:c.515A=
NM_015335.4:c.5902A=	NP_056150.1:p.Met1968=
XM_011538080.1:c.5938A=	XP_011536382.1:p.Met1980=
XM_011538081.1:c.5935A=	XP_011536383.1:p.Met1979=
XM_011538082.1:c.5908A=	XP_011536384.1:p.Met1970=
XM_011538080.2:c.5938A=	XP_011536382.1:p.Met1980=
XM_011538081.2:c.5935A=	XP_011536383.1:p.Met1979=
XM_011538082.2:c.5908A=	XP_011536384.1:p.Met1970=
XM_017019090.1:c.5899A=	XP_016874579.1:p.Met1967=
NM_015335.5:c.5902A= MANE Select	NP_056150.1:p.Met1968=