Canonical Allele Identifier: CA2065504371

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116237661C= , CM000674.2:g.116237661C=	GRCh38
NC_000012.11:g.116675466C= , CM000674.1:g.116675466C=	GRCh37
NC_000012.10:g.115159849C=	NCBI36
NG_023366.1:g.44526G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.117G= MANE Select	ENSP00000281928.3:p.Gly39=
ENST00000548743.2:c.87G=	ENSP00000448553.2:p.Gly29=
ENST00000551197.2:c.67G=
ENST00000647567.1:c.27G=	ENSP00000497136.1:p.Gly9=
ENST00000650226.1:c.117G=	ENSP00000496981.1:p.Gly39=
ENST00000650375.1:n.279G=
ENST00000281928.7:c.117G=	ENSP00000281928.3:p.Gly39=
ENST00000548743.1:c.87G=	ENSP00000448553.1:p.Gly29=
ENST00000551197.1:n.67G=
NM_015335.4:c.117G=	NP_056150.1:p.Gly39=
XM_011538080.1:c.117G=	XP_011536382.1:p.Gly39=
XM_011538081.1:c.117G=	XP_011536383.1:p.Gly39=
XM_011538082.1:c.87G=	XP_011536384.1:p.Gly29=
XM_011538080.2:c.117G=	XP_011536382.1:p.Gly39=
XM_011538081.2:c.117G=	XP_011536383.1:p.Gly39=
XM_011538082.2:c.87G=	XP_011536384.1:p.Gly29=
XM_017019090.1:c.117G=	XP_016874579.1:p.Gly39=
NM_015335.5:c.117G= MANE Select	NP_056150.1:p.Gly39=