Canonical Allele Identifier: CA2065385890

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991420G= , CM000674.2:g.115991420G=	GRCh38
NC_000012.11:g.116429225G= , CM000674.1:g.116429225G=	GRCh37
NC_000012.10:g.114913608G=	NCBI36
NG_023366.1:g.290767C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3534C= MANE Select	ENSP00000281928.3:p.Leu1178=
ENST00000549786.2:c.2962C=
ENST00000648379.1:n.1902C=
ENST00000648737.1:n.3298C=
ENST00000648825.1:n.274C=
ENST00000648916.1:n.1545C=
ENST00000649607.1:c.1718C=
ENST00000649775.1:c.31C=
ENST00000650226.1:c.3534C=	ENSP00000496981.1:p.Leu1178=
ENST00000281928.7:c.3534C=	ENSP00000281928.3:p.Leu1178=
NM_015335.4:c.3534C=	NP_056150.1:p.Leu1178=
XM_011538080.1:c.3534C=	XP_011536382.1:p.Leu1178=
XM_011538081.1:c.3531C=	XP_011536383.1:p.Leu1177=
XM_011538082.1:c.3504C=	XP_011536384.1:p.Leu1168=
XM_011538080.2:c.3534C=	XP_011536382.1:p.Leu1178=
XM_011538081.2:c.3531C=	XP_011536383.1:p.Leu1177=
XM_011538082.2:c.3504C=	XP_011536384.1:p.Leu1168=
XM_017019090.1:c.3531C=	XP_016874579.1:p.Leu1177=
NM_015335.5:c.3534C= MANE Select	NP_056150.1:p.Leu1178=