Canonical Allele Identifier: CA2065386301

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991644G= , CM000674.2:g.115991644G=	GRCh38
NC_000012.11:g.116429449G= , CM000674.1:g.116429449G=	GRCh37
NC_000012.10:g.114913832G=	NCBI36
NG_023366.1:g.290543C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3310C= MANE Select	ENSP00000281928.3:p.Pro1104=
ENST00000549786.2:c.2738C=
ENST00000648379.1:n.1678C=
ENST00000648737.1:n.3074C=
ENST00000648825.1:n.50C=
ENST00000648916.1:n.1321C=
ENST00000649607.1:c.1494C=
ENST00000650226.1:c.3310C=	ENSP00000496981.1:p.Pro1104=
ENST00000281928.7:c.3310C=	ENSP00000281928.3:p.Pro1104=
NM_015335.4:c.3310C=	NP_056150.1:p.Pro1104=
XM_011538080.1:c.3310C=	XP_011536382.1:p.Pro1104=
XM_011538081.1:c.3307C=	XP_011536383.1:p.Pro1103=
XM_011538082.1:c.3280C=	XP_011536384.1:p.Pro1094=
XM_011538080.2:c.3310C=	XP_011536382.1:p.Pro1104=
XM_011538081.2:c.3307C=	XP_011536383.1:p.Pro1103=
XM_011538082.2:c.3280C=	XP_011536384.1:p.Pro1094=
XM_017019090.1:c.3307C=	XP_016874579.1:p.Pro1103=
NM_015335.5:c.3310C= MANE Select	NP_056150.1:p.Pro1104=