Canonical Allele Identifier: CA2065381527

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116012844A= , CM000674.2:g.116012844A=	GRCh38
NC_000012.11:g.116450649A= , CM000674.1:g.116450649A=	GRCh37
NC_000012.10:g.114935032A=	NCBI36
NG_023366.1:g.269343T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.1233T= MANE Select	ENSP00000281928.3:p.Thr411=
ENST00000548743.2:c.1203T=	ENSP00000448553.2:p.Thr401=
ENST00000549786.2:c.661T=
ENST00000647567.1:c.1140T=	ENSP00000497136.1:p.Thr380=
ENST00000648737.1:n.997T=
ENST00000650226.1:c.1233T=	ENSP00000496981.1:p.Thr411=
ENST00000281928.7:c.1233T=	ENSP00000281928.3:p.Thr411=
NM_015335.4:c.1233T=	NP_056150.1:p.Thr411=
XM_011538080.1:c.1233T=	XP_011536382.1:p.Thr411=
XM_011538081.1:c.1233T=	XP_011536383.1:p.Thr411=
XM_011538082.1:c.1203T=	XP_011536384.1:p.Thr401=
XM_011538080.2:c.1233T=	XP_011536382.1:p.Thr411=
XM_011538081.2:c.1233T=	XP_011536383.1:p.Thr411=
XM_011538082.2:c.1203T=	XP_011536384.1:p.Thr401=
XM_017019090.1:c.1233T=	XP_016874579.1:p.Thr411=
NM_015335.5:c.1233T= MANE Select	NP_056150.1:p.Thr411=