Canonical Allele Identifier: CA2065398594

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116022481A= , CM000674.2:g.116022481A=	GRCh38
NC_000012.11:g.116460286A= , CM000674.1:g.116460286A=	GRCh37
NC_000012.10:g.114944669A=	NCBI36
NG_023366.1:g.259706T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.600T= MANE Select	ENSP00000281928.3:p.Ala200=
ENST00000548743.2:c.570T=	ENSP00000448553.2:p.Ala190=
ENST00000549786.2:c.28T=
ENST00000647567.1:c.510T=	ENSP00000497136.1:p.Ala170=
ENST00000648737.1:n.364T=
ENST00000650226.1:c.600T=	ENSP00000496981.1:p.Ala200=
ENST00000281928.7:c.600T=	ENSP00000281928.3:p.Ala200=
NM_015335.4:c.600T=	NP_056150.1:p.Ala200=
XM_011538080.1:c.600T=	XP_011536382.1:p.Ala200=
XM_011538081.1:c.600T=	XP_011536383.1:p.Ala200=
XM_011538082.1:c.570T=	XP_011536384.1:p.Ala190=
XM_011538080.2:c.600T=	XP_011536382.1:p.Ala200=
XM_011538081.2:c.600T=	XP_011536383.1:p.Ala200=
XM_011538082.2:c.570T=	XP_011536384.1:p.Ala190=
XM_017019090.1:c.600T=	XP_016874579.1:p.Ala200=
NM_015335.5:c.600T= MANE Select	NP_056150.1:p.Ala200=