Canonical Allele Identifier: CA2065375477

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984331T= , CM000674.2:g.115984331T=	GRCh38
NC_000012.11:g.116422136T= , CM000674.1:g.116422136T=	GRCh37
NC_000012.10:g.114906519T=	NCBI36
NG_023366.1:g.297856A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4380A= MANE Select	ENSP00000281928.3:p.Leu1460=
ENST00000549786.2:c.3808A=
ENST00000648379.1:n.2748A=
ENST00000648737.1:n.4144A=
ENST00000648825.1:n.1120A=
ENST00000648916.1:n.2391A=
ENST00000649146.1:n.1110A=
ENST00000649607.1:c.2564A=
ENST00000649775.1:c.877A=
ENST00000650091.1:n.2356A=
ENST00000650226.1:c.4380A=	ENSP00000496981.1:p.Leu1460=
ENST00000281928.7:c.4380A=	ENSP00000281928.3:p.Leu1460=
NM_015335.4:c.4380A=	NP_056150.1:p.Leu1460=
XM_011538080.1:c.4380A=	XP_011536382.1:p.Leu1460=
XM_011538081.1:c.4377A=	XP_011536383.1:p.Leu1459=
XM_011538082.1:c.4350A=	XP_011536384.1:p.Leu1450=
XM_011538080.2:c.4380A=	XP_011536382.1:p.Leu1460=
XM_011538081.2:c.4377A=	XP_011536383.1:p.Leu1459=
XM_011538082.2:c.4350A=	XP_011536384.1:p.Leu1450=
XM_017019090.1:c.4377A=	XP_016874579.1:p.Leu1459=
NM_015335.5:c.4380A= MANE Select	NP_056150.1:p.Leu1460=