Canonical Allele Identifier: CA2065381520

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116012840C= , CM000674.2:g.116012840C=	GRCh38
NC_000012.11:g.116450645C= , CM000674.1:g.116450645C=	GRCh37
NC_000012.10:g.114935028C=	NCBI36
NG_023366.1:g.269347G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.1237G= MANE Select	ENSP00000281928.3:p.Asp413=
ENST00000548743.2:c.1207G=	ENSP00000448553.2:p.Asp403=
ENST00000549786.2:c.665G=
ENST00000647567.1:c.1144G=	ENSP00000497136.1:p.Asp382=
ENST00000648737.1:n.1001G=
ENST00000650226.1:c.1237G=	ENSP00000496981.1:p.Asp413=
ENST00000281928.7:c.1237G=	ENSP00000281928.3:p.Asp413=
NM_015335.4:c.1237G=	NP_056150.1:p.Asp413=
XM_011538080.1:c.1237G=	XP_011536382.1:p.Asp413=
XM_011538081.1:c.1237G=	XP_011536383.1:p.Asp413=
XM_011538082.1:c.1207G=	XP_011536384.1:p.Asp403=
XM_011538080.2:c.1237G=	XP_011536382.1:p.Asp413=
XM_011538081.2:c.1237G=	XP_011536383.1:p.Asp413=
XM_011538082.2:c.1207G=	XP_011536384.1:p.Asp403=
XM_017019090.1:c.1237G=	XP_016874579.1:p.Asp413=
NM_015335.5:c.1237G= MANE Select	NP_056150.1:p.Asp413=