Canonical Allele Identifier: CA2065412927

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975302C= , CM000674.2:g.115975302C=	GRCh38
NC_000012.11:g.116413107C= , CM000674.1:g.116413107C=	GRCh37
NC_000012.10:g.114897490C=	NCBI36
NG_023366.1:g.306885G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5600G= MANE Select	ENSP00000281928.3:p.Ser1867=
ENST00000548694.2:n.590G=
ENST00000648379.1:n.3968G=
ENST00000648737.1:n.5364G=
ENST00000648825.1:n.3785G=
ENST00000648916.1:n.3611G=
ENST00000649607.1:c.3784G=
ENST00000649775.1:c.2089G=
ENST00000650226.1:c.5636G=	ENSP00000496981.1:p.Ser1879=
ENST00000281928.7:c.5600G=	ENSP00000281928.3:p.Ser1867=
ENST00000548694.1:n.590G=
ENST00000552447.1:c.213G=
NM_015335.4:c.5600G=	NP_056150.1:p.Ser1867=
XM_011538080.1:c.5636G=	XP_011536382.1:p.Ser1879=
XM_011538081.1:c.5633G=	XP_011536383.1:p.Ser1878=
XM_011538082.1:c.5606G=	XP_011536384.1:p.Ser1869=
XM_011538080.2:c.5636G=	XP_011536382.1:p.Ser1879=
XM_011538081.2:c.5633G=	XP_011536383.1:p.Ser1878=
XM_011538082.2:c.5606G=	XP_011536384.1:p.Ser1869=
XM_017019090.1:c.5597G=	XP_016874579.1:p.Ser1866=
NM_015335.5:c.5600G= MANE Select	NP_056150.1:p.Ser1867=