Canonical Allele Identifier: CA2065396859

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997202G= , CM000674.2:g.115997202G=	GRCh38
NC_000012.11:g.116435007G= , CM000674.1:g.116435007G=	GRCh37
NC_000012.10:g.114919390G=	NCBI36
NG_023366.1:g.284985C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2598C= MANE Select	ENSP00000281928.3:p.Pro866=
ENST00000548743.2:c.2568C=	ENSP00000448553.2:p.Pro856=
ENST00000549786.2:c.2026C=
ENST00000647927.1:n.2971C=
ENST00000648173.1:n.1393C=
ENST00000648379.1:n.966C=
ENST00000648737.1:n.2362C=
ENST00000648916.1:n.609C=
ENST00000649607.1:c.782C=
ENST00000650226.1:c.2598C=	ENSP00000496981.1:p.Pro866=
ENST00000281928.7:c.2598C=	ENSP00000281928.3:p.Pro866=
NM_015335.4:c.2598C=	NP_056150.1:p.Pro866=
XM_011538080.1:c.2598C=	XP_011536382.1:p.Pro866=
XM_011538081.1:c.2595C=	XP_011536383.1:p.Pro865=
XM_011538082.1:c.2568C=	XP_011536384.1:p.Pro856=
XM_011538080.2:c.2598C=	XP_011536382.1:p.Pro866=
XM_011538081.2:c.2595C=	XP_011536383.1:p.Pro865=
XM_011538082.2:c.2568C=	XP_011536384.1:p.Pro856=
XM_017019090.1:c.2595C=	XP_016874579.1:p.Pro865=
NM_015335.5:c.2598C= MANE Select	NP_056150.1:p.Pro866=