Canonical Allele Identifier: CA2065410930

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970751A= , CM000674.2:g.115970751A=	GRCh38
NC_000012.11:g.116408556A= , CM000674.1:g.116408556A=	GRCh37
NC_000012.10:g.114892939A=	NCBI36
NG_023366.1:g.311436T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5910T= MANE Select	ENSP00000281928.3:p.Ser1970=
ENST00000548784.2:n.2124T=
ENST00000648379.1:n.4278T=
ENST00000648737.1:n.5674T=
ENST00000648825.1:n.4095T=
ENST00000648916.1:n.3921T=
ENST00000649607.1:c.4094T=
ENST00000649775.1:c.2399T=
ENST00000650226.1:c.5946T=	ENSP00000496981.1:p.Ser1982=
ENST00000281928.7:c.5910T=	ENSP00000281928.3:p.Ser1970=
ENST00000548784.1:n.408T=
ENST00000552447.1:c.523T=
NM_015335.4:c.5910T=	NP_056150.1:p.Ser1970=
XM_011538080.1:c.5946T=	XP_011536382.1:p.Ser1982=
XM_011538081.1:c.5943T=	XP_011536383.1:p.Ser1981=
XM_011538082.1:c.5916T=	XP_011536384.1:p.Ser1972=
XM_011538080.2:c.5946T=	XP_011536382.1:p.Ser1982=
XM_011538081.2:c.5943T=	XP_011536383.1:p.Ser1981=
XM_011538082.2:c.5916T=	XP_011536384.1:p.Ser1972=
XM_017019090.1:c.5907T=	XP_016874579.1:p.Ser1969=
NM_015335.5:c.5910T= MANE Select	NP_056150.1:p.Ser1970=