Canonical Allele Identifier: CA2065386390

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991662C= , CM000674.2:g.115991662C=	GRCh38
NC_000012.11:g.116429467C= , CM000674.1:g.116429467C=	GRCh37
NC_000012.10:g.114913850C=	NCBI36
NG_023366.1:g.290525G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3292G= MANE Select	ENSP00000281928.3:p.Ala1098=
ENST00000549786.2:c.2720G=
ENST00000648379.1:n.1660G=
ENST00000648737.1:n.3056G=
ENST00000648825.1:n.32G=
ENST00000648916.1:n.1303G=
ENST00000649607.1:c.1476G=
ENST00000650226.1:c.3292G=	ENSP00000496981.1:p.Ala1098=
ENST00000281928.7:c.3292G=	ENSP00000281928.3:p.Ala1098=
NM_015335.4:c.3292G=	NP_056150.1:p.Ala1098=
XM_011538080.1:c.3292G=	XP_011536382.1:p.Ala1098=
XM_011538081.1:c.3289G=	XP_011536383.1:p.Ala1097=
XM_011538082.1:c.3262G=	XP_011536384.1:p.Ala1088=
XM_011538080.2:c.3292G=	XP_011536382.1:p.Ala1098=
XM_011538081.2:c.3289G=	XP_011536383.1:p.Ala1097=
XM_011538082.2:c.3262G=	XP_011536384.1:p.Ala1088=
XM_017019090.1:c.3289G=	XP_016874579.1:p.Ala1097=
NM_015335.5:c.3292G= MANE Select	NP_056150.1:p.Ala1098=