Canonical Allele Identifier: CA2065371532

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982478G= , CM000674.2:g.115982478G=	GRCh38
NC_000012.11:g.116420283G= , CM000674.1:g.116420283G=	GRCh37
NC_000012.10:g.114904666G=	NCBI36
NG_023366.1:g.299709C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5081C= MANE Select	ENSP00000281928.3:p.Thr1694=
ENST00000549786.2:c.4509C=
ENST00000648379.1:n.3449C=
ENST00000648737.1:n.4845C=
ENST00000648825.1:n.1821C=
ENST00000648916.1:n.3092C=
ENST00000649146.1:n.2324C=
ENST00000649607.1:c.3265C=
ENST00000649775.1:c.1570C=
ENST00000650226.1:c.5081C=	ENSP00000496981.1:p.Thr1694=
ENST00000281928.7:c.5081C=	ENSP00000281928.3:p.Thr1694=
ENST00000549786.1:c.445C=
ENST00000552340.1:c.113C=	ENSP00000449876.1:p.Thr38=
NM_015335.4:c.5081C=	NP_056150.1:p.Thr1694=
XM_011538080.1:c.5081C=	XP_011536382.1:p.Thr1694=
XM_011538081.1:c.5078C=	XP_011536383.1:p.Thr1693=
XM_011538082.1:c.5051C=	XP_011536384.1:p.Thr1684=
XM_011538080.2:c.5081C=	XP_011536382.1:p.Thr1694=
XM_011538081.2:c.5078C=	XP_011536383.1:p.Thr1693=
XM_011538082.2:c.5051C=	XP_011536384.1:p.Thr1684=
XM_017019090.1:c.5078C=	XP_016874579.1:p.Thr1693=
NM_015335.5:c.5081C= MANE Select	NP_056150.1:p.Thr1694=