Canonical Allele Identifier: CA2065386452

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991671C= , CM000674.2:g.115991671C=	GRCh38
NC_000012.11:g.116429476C= , CM000674.1:g.116429476C=	GRCh37
NC_000012.10:g.114913859C=	NCBI36
NG_023366.1:g.290516G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3283G= MANE Select	ENSP00000281928.3:p.Val1095=
ENST00000549786.2:c.2711G=
ENST00000648379.1:n.1651G=
ENST00000648737.1:n.3047G=
ENST00000648825.1:n.23G=
ENST00000648916.1:n.1294G=
ENST00000649607.1:c.1467G=
ENST00000650226.1:c.3283G=	ENSP00000496981.1:p.Val1095=
ENST00000281928.7:c.3283G=	ENSP00000281928.3:p.Val1095=
NM_015335.4:c.3283G=	NP_056150.1:p.Val1095=
XM_011538080.1:c.3283G=	XP_011536382.1:p.Val1095=
XM_011538081.1:c.3280G=	XP_011536383.1:p.Val1094=
XM_011538082.1:c.3253G=	XP_011536384.1:p.Val1085=
XM_011538080.2:c.3283G=	XP_011536382.1:p.Val1095=
XM_011538081.2:c.3280G=	XP_011536383.1:p.Val1094=
XM_011538082.2:c.3253G=	XP_011536384.1:p.Val1085=
XM_017019090.1:c.3280G=	XP_016874579.1:p.Val1094=
NM_015335.5:c.3283G= MANE Select	NP_056150.1:p.Val1095=