Canonical Allele Identifier: CA2065371547

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982493G= , CM000674.2:g.115982493G=	GRCh38
NC_000012.11:g.116420298G= , CM000674.1:g.116420298G=	GRCh37
NC_000012.10:g.114904681G=	NCBI36
NG_023366.1:g.299694C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5066C= MANE Select	ENSP00000281928.3:p.Ala1689=
ENST00000549786.2:c.4494C=
ENST00000648379.1:n.3434C=
ENST00000648737.1:n.4830C=
ENST00000648825.1:n.1806C=
ENST00000648916.1:n.3077C=
ENST00000649146.1:n.2309C=
ENST00000649607.1:c.3250C=
ENST00000649775.1:c.1555C=
ENST00000650226.1:c.5066C=	ENSP00000496981.1:p.Ala1689=
ENST00000281928.7:c.5066C=	ENSP00000281928.3:p.Ala1689=
ENST00000549786.1:c.430C=
ENST00000552340.1:c.98C=	ENSP00000449876.1:p.Ala33=
NM_015335.4:c.5066C=	NP_056150.1:p.Ala1689=
XM_011538080.1:c.5066C=	XP_011536382.1:p.Ala1689=
XM_011538081.1:c.5063C=	XP_011536383.1:p.Ala1688=
XM_011538082.1:c.5036C=	XP_011536384.1:p.Ala1679=
XM_011538080.2:c.5066C=	XP_011536382.1:p.Ala1689=
XM_011538081.2:c.5063C=	XP_011536383.1:p.Ala1688=
XM_011538082.2:c.5036C=	XP_011536384.1:p.Ala1679=
XM_017019090.1:c.5063C=	XP_016874579.1:p.Ala1688=
NM_015335.5:c.5066C= MANE Select	NP_056150.1:p.Ala1689=