Canonical Allele Identifier: CA2065504294

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116237618C= , CM000674.2:g.116237618C=	GRCh38
NC_000012.11:g.116675423C= , CM000674.1:g.116675423C=	GRCh37
NC_000012.10:g.115159806C=	NCBI36
NG_023366.1:g.44569G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.160G= MANE Select	ENSP00000281928.3:p.Asp54=
ENST00000548743.2:c.130G=	ENSP00000448553.2:p.Asp44=
ENST00000551197.2:c.110G=
ENST00000647567.1:c.70G=	ENSP00000497136.1:p.Asp24=
ENST00000650226.1:c.160G=	ENSP00000496981.1:p.Asp54=
ENST00000650375.1:n.322G=
ENST00000281928.7:c.160G=	ENSP00000281928.3:p.Asp54=
ENST00000548743.1:c.130G=	ENSP00000448553.1:p.Asp44=
ENST00000551197.1:n.110G=
NM_015335.4:c.160G=	NP_056150.1:p.Asp54=
XM_011538080.1:c.160G=	XP_011536382.1:p.Asp54=
XM_011538081.1:c.160G=	XP_011536383.1:p.Asp54=
XM_011538082.1:c.130G=	XP_011536384.1:p.Asp44=
XM_011538080.2:c.160G=	XP_011536382.1:p.Asp54=
XM_011538081.2:c.160G=	XP_011536383.1:p.Asp54=
XM_011538082.2:c.130G=	XP_011536384.1:p.Asp44=
XM_017019090.1:c.160G=	XP_016874579.1:p.Asp54=
NM_015335.5:c.160G= MANE Select	NP_056150.1:p.Asp54=