Canonical Allele Identifier: CA2065504484

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116237752G= , CM000674.2:g.116237752G=	GRCh38
NC_000012.11:g.116675557G= , CM000674.1:g.116675557G=	GRCh37
NC_000012.10:g.115159940G=	NCBI36
NG_023366.1:g.44435C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.73-47C= MANE Select	ENSP00000281928.3:n.73-47C=
ENST00000548743.2:c.43-47C=	ENSP00000448553.2:n.43-47C=
ENST00000551197.2:c.23-47C=
ENST00000650226.1:c.73-47C=	ENSP00000496981.1:n.73-47C=
ENST00000650375.1:n.235-47C=
ENST00000281928.7:c.73-47C=	ENSP00000281928.3:n.73-47C=
ENST00000548743.1:c.43-47C=	ENSP00000448553.1:n.43-47C=
ENST00000551197.1:n.23-47C=
NM_015335.4:c.73-47C=	NP_056150.1:n.73-47C=
XM_011538080.1:c.73-47C=	XP_011536382.1:n.73-47C=
XM_011538081.1:c.73-47C=	XP_011536383.1:n.73-47C=
XM_011538082.1:c.43-47C=	XP_011536384.1:n.43-47C=
XM_011538080.2:c.73-47C=	XP_011536382.1:n.73-47C=
XM_011538081.2:c.73-47C=	XP_011536383.1:n.73-47C=
XM_011538082.2:c.43-47C=	XP_011536384.1:n.43-47C=
XM_017019090.1:c.73-47C=	XP_016874579.1:n.73-47C=
NM_015335.5:c.73-47C= MANE Select	NP_056150.1:n.73-47C=