Canonical Allele Identifier: CA2065371825

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982583A= , CM000674.2:g.115982583A=	GRCh38
NC_000012.11:g.116420388A= , CM000674.1:g.116420388A=	GRCh37
NC_000012.10:g.114904771A=	NCBI36
NG_023366.1:g.299604T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4976T= MANE Select	ENSP00000281928.3:p.Ile1659=
ENST00000549786.2:c.4404T=
ENST00000648379.1:n.3344T=
ENST00000648737.1:n.4740T=
ENST00000648825.1:n.1716T=
ENST00000648916.1:n.2987T=
ENST00000649146.1:n.2219T=
ENST00000649607.1:c.3160T=
ENST00000649775.1:c.1465T=
ENST00000650226.1:c.4976T=	ENSP00000496981.1:p.Ile1659=
ENST00000281928.7:c.4976T=	ENSP00000281928.3:p.Ile1659=
ENST00000549786.1:c.340T=
ENST00000552340.1:c.8T=	ENSP00000449876.1:p.Ile3=
NM_015335.4:c.4976T=	NP_056150.1:p.Ile1659=
XM_011538080.1:c.4976T=	XP_011536382.1:p.Ile1659=
XM_011538081.1:c.4973T=	XP_011536383.1:p.Ile1658=
XM_011538082.1:c.4946T=	XP_011536384.1:p.Ile1649=
XM_011538080.2:c.4976T=	XP_011536382.1:p.Ile1659=
XM_011538081.2:c.4973T=	XP_011536383.1:p.Ile1658=
XM_011538082.2:c.4946T=	XP_011536384.1:p.Ile1649=
XM_017019090.1:c.4973T=	XP_016874579.1:p.Ile1658=
NM_015335.5:c.4976T= MANE Select	NP_056150.1:p.Ile1659=