Canonical Allele Identifier: CA2065371763

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982558A= , CM000674.2:g.115982558A=	GRCh38
NC_000012.11:g.116420363A= , CM000674.1:g.116420363A=	GRCh37
NC_000012.10:g.114904746A=	NCBI36
NG_023366.1:g.299629T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5001T= MANE Select	ENSP00000281928.3:p.Ser1667=
ENST00000549786.2:c.4429T=
ENST00000648379.1:n.3369T=
ENST00000648737.1:n.4765T=
ENST00000648825.1:n.1741T=
ENST00000648916.1:n.3012T=
ENST00000649146.1:n.2244T=
ENST00000649607.1:c.3185T=
ENST00000649775.1:c.1490T=
ENST00000650226.1:c.5001T=	ENSP00000496981.1:p.Ser1667=
ENST00000281928.7:c.5001T=	ENSP00000281928.3:p.Ser1667=
ENST00000549786.1:c.365T=
ENST00000552340.1:c.33T=	ENSP00000449876.1:p.Ser11=
NM_015335.4:c.5001T=	NP_056150.1:p.Ser1667=
XM_011538080.1:c.5001T=	XP_011536382.1:p.Ser1667=
XM_011538081.1:c.4998T=	XP_011536383.1:p.Ser1666=
XM_011538082.1:c.4971T=	XP_011536384.1:p.Ser1657=
XM_011538080.2:c.5001T=	XP_011536382.1:p.Ser1667=
XM_011538081.2:c.4998T=	XP_011536383.1:p.Ser1666=
XM_011538082.2:c.4971T=	XP_011536384.1:p.Ser1657=
XM_017019090.1:c.4998T=	XP_016874579.1:p.Ser1666=
NM_015335.5:c.5001T= MANE Select	NP_056150.1:p.Ser1667=