Canonical Allele Identifier: CA2065410924

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970719T= , CM000674.2:g.115970719T=	GRCh38
NC_000012.11:g.116408524T= , CM000674.1:g.116408524T=	GRCh37
NC_000012.10:g.114892907T=	NCBI36
NG_023366.1:g.311468A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5942A= MANE Select	ENSP00000281928.3:p.Gln1981=
ENST00000548784.2:n.2156A=
ENST00000648379.1:n.4310A=
ENST00000648737.1:n.5706A=
ENST00000648825.1:n.4127A=
ENST00000648916.1:n.3953A=
ENST00000649607.1:c.4126A=
ENST00000649775.1:c.2431A=
ENST00000650226.1:c.5978A=	ENSP00000496981.1:p.Gln1993=
ENST00000281928.7:c.5942A=	ENSP00000281928.3:p.Gln1981=
ENST00000548784.1:n.440A=
ENST00000552447.1:c.555A=
NM_015335.4:c.5942A=	NP_056150.1:p.Gln1981=
XM_011538080.1:c.5978A=	XP_011536382.1:p.Gln1993=
XM_011538081.1:c.5975A=	XP_011536383.1:p.Gln1992=
XM_011538082.1:c.5948A=	XP_011536384.1:p.Gln1983=
XM_011538080.2:c.5978A=	XP_011536382.1:p.Gln1993=
XM_011538081.2:c.5975A=	XP_011536383.1:p.Gln1992=
XM_011538082.2:c.5948A=	XP_011536384.1:p.Gln1983=
XM_017019090.1:c.5939A=	XP_016874579.1:p.Gln1980=
NM_015335.5:c.5942A= MANE Select	NP_056150.1:p.Gln1981=