Canonical Allele Identifier: CA2065398547

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116022458T= , CM000674.2:g.116022458T=	GRCh38
NC_000012.11:g.116460263T= , CM000674.1:g.116460263T=	GRCh37
NC_000012.10:g.114944646T=	NCBI36
NG_023366.1:g.259729A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.623A= MANE Select	ENSP00000281928.3:p.Gln208=
ENST00000548743.2:c.593A=	ENSP00000448553.2:p.Gln198=
ENST00000549786.2:c.51A=
ENST00000647567.1:c.533A=	ENSP00000497136.1:p.Gln178=
ENST00000648737.1:n.387A=
ENST00000650226.1:c.623A=	ENSP00000496981.1:p.Gln208=
ENST00000281928.7:c.623A=	ENSP00000281928.3:p.Gln208=
NM_015335.4:c.623A=	NP_056150.1:p.Gln208=
XM_011538080.1:c.623A=	XP_011536382.1:p.Gln208=
XM_011538081.1:c.623A=	XP_011536383.1:p.Gln208=
XM_011538082.1:c.593A=	XP_011536384.1:p.Gln198=
XM_011538080.2:c.623A=	XP_011536382.1:p.Gln208=
XM_011538081.2:c.623A=	XP_011536383.1:p.Gln208=
XM_011538082.2:c.593A=	XP_011536384.1:p.Gln198=
XM_017019090.1:c.623A=	XP_016874579.1:p.Gln208=
NM_015335.5:c.623A= MANE Select	NP_056150.1:p.Gln208=