Canonical Allele Identifier: CA2065412915

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975274T= , CM000674.2:g.115975274T=	GRCh38
NC_000012.11:g.116413079T= , CM000674.1:g.116413079T=	GRCh37
NC_000012.10:g.114897462T=	NCBI36
NG_023366.1:g.306913A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5628A= MANE Select	ENSP00000281928.3:p.Leu1876=
ENST00000548694.2:n.618A=
ENST00000648379.1:n.3996A=
ENST00000648737.1:n.5392A=
ENST00000648825.1:n.3813A=
ENST00000648916.1:n.3639A=
ENST00000649607.1:c.3812A=
ENST00000649775.1:c.2117A=
ENST00000650226.1:c.5664A=	ENSP00000496981.1:p.Leu1888=
ENST00000281928.7:c.5628A=	ENSP00000281928.3:p.Leu1876=
ENST00000548694.1:n.618A=
ENST00000552447.1:c.241A=
NM_015335.4:c.5628A=	NP_056150.1:p.Leu1876=
XM_011538080.1:c.5664A=	XP_011536382.1:p.Leu1888=
XM_011538081.1:c.5661A=	XP_011536383.1:p.Leu1887=
XM_011538082.1:c.5634A=	XP_011536384.1:p.Leu1878=
XM_011538080.2:c.5664A=	XP_011536382.1:p.Leu1888=
XM_011538081.2:c.5661A=	XP_011536383.1:p.Leu1887=
XM_011538082.2:c.5634A=	XP_011536384.1:p.Leu1878=
XM_017019090.1:c.5625A=	XP_016874579.1:p.Leu1875=
NM_015335.5:c.5628A= MANE Select	NP_056150.1:p.Leu1876=