Canonical Allele Identifier: CA2065396961

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997227A= , CM000674.2:g.115997227A=	GRCh38
NC_000012.11:g.116435032A= , CM000674.1:g.116435032A=	GRCh37
NC_000012.10:g.114919415A=	NCBI36
NG_023366.1:g.284960T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2573T= MANE Select	ENSP00000281928.3:p.Val858=
ENST00000548743.2:c.2543T=	ENSP00000448553.2:p.Val848=
ENST00000549786.2:c.2001T=
ENST00000647927.1:n.2946T=
ENST00000648173.1:n.1368T=
ENST00000648379.1:n.941T=
ENST00000648737.1:n.2337T=
ENST00000648916.1:n.584T=
ENST00000649607.1:c.757T=
ENST00000650226.1:c.2573T=	ENSP00000496981.1:p.Val858=
ENST00000281928.7:c.2573T=	ENSP00000281928.3:p.Val858=
NM_015335.4:c.2573T=	NP_056150.1:p.Val858=
XM_011538080.1:c.2573T=	XP_011536382.1:p.Val858=
XM_011538081.1:c.2570T=	XP_011536383.1:p.Ile857=
XM_011538082.1:c.2543T=	XP_011536384.1:p.Val848=
XM_011538080.2:c.2573T=	XP_011536382.1:p.Val858=
XM_011538081.2:c.2570T=	XP_011536383.1:p.Ile857=
XM_011538082.2:c.2543T=	XP_011536384.1:p.Val848=
XM_017019090.1:c.2570T=	XP_016874579.1:p.Ile857=
NM_015335.5:c.2573T= MANE Select	NP_056150.1:p.Val858=