Canonical Allele Identifier: CA2065396022

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115996760A= , CM000674.2:g.115996760A=	GRCh38
NC_000012.11:g.116434565A= , CM000674.1:g.116434565A=	GRCh37
NC_000012.10:g.114918948A=	NCBI36
NG_023366.1:g.285427T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2791-79T= MANE Select	ENSP00000281928.3:n.2791-79T=
ENST00000548743.2:c.2761-79T=	ENSP00000448553.2:n.2761-79T=
ENST00000549786.2:c.2219-79T=
ENST00000647927.1:n.3164-79T=
ENST00000648173.1:n.1586-79T=
ENST00000648379.1:n.1159-79T=
ENST00000648737.1:n.2555-79T=
ENST00000648916.1:n.802-79T=
ENST00000649607.1:c.975-79T=
ENST00000650226.1:c.2791-79T=	ENSP00000496981.1:n.2791-79T=
ENST00000281928.7:c.2791-79T=	ENSP00000281928.3:n.2791-79T=
NM_015335.4:c.2791-79T=	NP_056150.1:n.2791-79T=
XM_011538080.1:c.2791-79T=	XP_011536382.1:n.2791-79T=
XM_011538081.1:c.2788-79T=	XP_011536383.1:n.2788-79T=
XM_011538082.1:c.2761-79T=	XP_011536384.1:n.2761-79T=
XM_011538080.2:c.2791-79T=	XP_011536382.1:n.2791-79T=
XM_011538081.2:c.2788-79T=	XP_011536383.1:n.2788-79T=
XM_011538082.2:c.2761-79T=	XP_011536384.1:n.2761-79T=
XM_017019090.1:c.2788-79T=	XP_016874579.1:n.2788-79T=
NM_015335.5:c.2791-79T= MANE Select	NP_056150.1:n.2791-79T=