Canonical Allele Identifier: CA2065412892

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975194C= , CM000674.2:g.115975194C=	GRCh38
NC_000012.11:g.116412999C= , CM000674.1:g.116412999C=	GRCh37
NC_000012.10:g.114897382C=	NCBI36
NG_023366.1:g.306993G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5708G= MANE Select	ENSP00000281928.3:p.Arg1903=
ENST00000548694.2:n.698G=
ENST00000648379.1:n.4076G=
ENST00000648737.1:n.5472G=
ENST00000648825.1:n.3893G=
ENST00000648916.1:n.3719G=
ENST00000649607.1:c.3892G=
ENST00000649775.1:c.2197G=
ENST00000650226.1:c.5744G=	ENSP00000496981.1:p.Arg1915=
ENST00000281928.7:c.5708G=	ENSP00000281928.3:p.Arg1903=
ENST00000548694.1:n.698G=
ENST00000552447.1:c.321G=
NM_015335.4:c.5708G=	NP_056150.1:p.Arg1903=
XM_011538080.1:c.5744G=	XP_011536382.1:p.Arg1915=
XM_011538081.1:c.5741G=	XP_011536383.1:p.Arg1914=
XM_011538082.1:c.5714G=	XP_011536384.1:p.Arg1905=
XM_011538080.2:c.5744G=	XP_011536382.1:p.Arg1915=
XM_011538081.2:c.5741G=	XP_011536383.1:p.Arg1914=
XM_011538082.2:c.5714G=	XP_011536384.1:p.Arg1905=
XM_017019090.1:c.5705G=	XP_016874579.1:p.Arg1902=
NM_015335.5:c.5708G= MANE Select	NP_056150.1:p.Arg1903=