Canonical Allele Identifier: CA2065371585

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982499T= , CM000674.2:g.115982499T=	GRCh38
NC_000012.11:g.116420304T= , CM000674.1:g.116420304T=	GRCh37
NC_000012.10:g.114904687T=	NCBI36
NG_023366.1:g.299688A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5060A= MANE Select	ENSP00000281928.3:p.Tyr1687=
ENST00000549786.2:c.4488A=
ENST00000648379.1:n.3428A=
ENST00000648737.1:n.4824A=
ENST00000648825.1:n.1800A=
ENST00000648916.1:n.3071A=
ENST00000649146.1:n.2303A=
ENST00000649607.1:c.3244A=
ENST00000649775.1:c.1549A=
ENST00000650226.1:c.5060A=	ENSP00000496981.1:p.Tyr1687=
ENST00000281928.7:c.5060A=	ENSP00000281928.3:p.Tyr1687=
ENST00000549786.1:c.424A=
ENST00000552340.1:c.92A=	ENSP00000449876.1:p.Tyr31=
NM_015335.4:c.5060A=	NP_056150.1:p.Tyr1687=
XM_011538080.1:c.5060A=	XP_011536382.1:p.Tyr1687=
XM_011538081.1:c.5057A=	XP_011536383.1:p.Tyr1686=
XM_011538082.1:c.5030A=	XP_011536384.1:p.Tyr1677=
XM_011538080.2:c.5060A=	XP_011536382.1:p.Tyr1687=
XM_011538081.2:c.5057A=	XP_011536383.1:p.Tyr1686=
XM_011538082.2:c.5030A=	XP_011536384.1:p.Tyr1677=
XM_017019090.1:c.5057A=	XP_016874579.1:p.Tyr1686=
NM_015335.5:c.5060A= MANE Select	NP_056150.1:p.Tyr1687=