Canonical Allele Identifier: CA2065398557

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116022471G= , CM000674.2:g.116022471G=	GRCh38
NC_000012.11:g.116460276G= , CM000674.1:g.116460276G=	GRCh37
NC_000012.10:g.114944659G=	NCBI36
NG_023366.1:g.259716C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.610C= MANE Select	ENSP00000281928.3:p.Pro204=
ENST00000548743.2:c.580C=	ENSP00000448553.2:p.Pro194=
ENST00000549786.2:c.38C=
ENST00000647567.1:c.520C=	ENSP00000497136.1:p.Pro174=
ENST00000648737.1:n.374C=
ENST00000650226.1:c.610C=	ENSP00000496981.1:p.Pro204=
ENST00000281928.7:c.610C=	ENSP00000281928.3:p.Pro204=
NM_015335.4:c.610C=	NP_056150.1:p.Pro204=
XM_011538080.1:c.610C=	XP_011536382.1:p.Pro204=
XM_011538081.1:c.610C=	XP_011536383.1:p.Pro204=
XM_011538082.1:c.580C=	XP_011536384.1:p.Pro194=
XM_011538080.2:c.610C=	XP_011536382.1:p.Pro204=
XM_011538081.2:c.610C=	XP_011536383.1:p.Pro204=
XM_011538082.2:c.580C=	XP_011536384.1:p.Pro194=
XM_017019090.1:c.610C=	XP_016874579.1:p.Pro204=
NM_015335.5:c.610C= MANE Select	NP_056150.1:p.Pro204=