Canonical Allele Identifier: CA2065386570

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991701T= , CM000674.2:g.115991701T=	GRCh38
NC_000012.11:g.116429506T= , CM000674.1:g.116429506T=	GRCh37
NC_000012.10:g.114913889T=	NCBI36
NG_023366.1:g.290486A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.3253A= MANE Select	ENSP00000281928.3:p.Thr1085=
ENST00000548743.2:c.3223A=	ENSP00000448553.2:p.Thr1075=
ENST00000549786.2:c.2681A=
ENST00000648173.1:n.2048A=
ENST00000648379.1:n.1621A=
ENST00000648737.1:n.3017A=
ENST00000648916.1:n.1264A=
ENST00000649607.1:c.1437A=
ENST00000650226.1:c.3253A=	ENSP00000496981.1:p.Thr1085=
ENST00000281928.7:c.3253A=	ENSP00000281928.3:p.Thr1085=
NM_015335.4:c.3253A=	NP_056150.1:p.Thr1085=
XM_011538080.1:c.3253A=	XP_011536382.1:p.Thr1085=
XM_011538081.1:c.3250A=	XP_011536383.1:p.Thr1084=
XM_011538082.1:c.3223A=	XP_011536384.1:p.Thr1075=
XM_011538080.2:c.3253A=	XP_011536382.1:p.Thr1085=
XM_011538081.2:c.3250A=	XP_011536383.1:p.Thr1084=
XM_011538082.2:c.3223A=	XP_011536384.1:p.Thr1075=
XM_017019090.1:c.3250A=	XP_016874579.1:p.Thr1084=
NM_015335.5:c.3253A= MANE Select	NP_056150.1:p.Thr1085=