Canonical Allele Identifier: CA2065387080

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991911T= , CM000674.2:g.115991911T=	GRCh38
NC_000012.11:g.116429716T= , CM000674.1:g.116429716T=	GRCh37
NC_000012.10:g.114914099T=	NCBI36
NG_023366.1:g.290276A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3043A= MANE Select	ENSP00000281928.3:p.Thr1015=
ENST00000548743.2:c.3013A=	ENSP00000448553.2:p.Thr1005=
ENST00000549786.2:c.2471A=
ENST00000648173.1:n.1838A=
ENST00000648379.1:n.1411A=
ENST00000648737.1:n.2807A=
ENST00000648916.1:n.1054A=
ENST00000649607.1:c.1227A=
ENST00000650226.1:c.3043A=	ENSP00000496981.1:p.Thr1015=
ENST00000281928.7:c.3043A=	ENSP00000281928.3:p.Thr1015=
NM_015335.4:c.3043A=	NP_056150.1:p.Thr1015=
XM_011538080.1:c.3043A=	XP_011536382.1:p.Thr1015=
XM_011538081.1:c.3040A=	XP_011536383.1:p.Thr1014=
XM_011538082.1:c.3013A=	XP_011536384.1:p.Thr1005=
XM_011538080.2:c.3043A=	XP_011536382.1:p.Thr1015=
XM_011538081.2:c.3040A=	XP_011536383.1:p.Thr1014=
XM_011538082.2:c.3013A=	XP_011536384.1:p.Thr1005=
XM_017019090.1:c.3040A=	XP_016874579.1:p.Thr1014=
NM_015335.5:c.3043A= MANE Select	NP_056150.1:p.Thr1015=