Canonical Allele Identifier: CA2065371797

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982570C= , CM000674.2:g.115982570C=	GRCh38
NC_000012.11:g.116420375C= , CM000674.1:g.116420375C=	GRCh37
NC_000012.10:g.114904758C=	NCBI36
NG_023366.1:g.299617G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4989G= MANE Select	ENSP00000281928.3:p.Thr1663=
ENST00000549786.2:c.4417G=
ENST00000648379.1:n.3357G=
ENST00000648737.1:n.4753G=
ENST00000648825.1:n.1729G=
ENST00000648916.1:n.3000G=
ENST00000649146.1:n.2232G=
ENST00000649607.1:c.3173G=
ENST00000649775.1:c.1478G=
ENST00000650226.1:c.4989G=	ENSP00000496981.1:p.Thr1663=
ENST00000281928.7:c.4989G=	ENSP00000281928.3:p.Thr1663=
ENST00000549786.1:c.353G=
ENST00000552340.1:c.21G=	ENSP00000449876.1:p.Thr7=
NM_015335.4:c.4989G=	NP_056150.1:p.Thr1663=
XM_011538080.1:c.4989G=	XP_011536382.1:p.Thr1663=
XM_011538081.1:c.4986G=	XP_011536383.1:p.Thr1662=
XM_011538082.1:c.4959G=	XP_011536384.1:p.Thr1653=
XM_011538080.2:c.4989G=	XP_011536382.1:p.Thr1663=
XM_011538081.2:c.4986G=	XP_011536383.1:p.Thr1662=
XM_011538082.2:c.4959G=	XP_011536384.1:p.Thr1653=
XM_017019090.1:c.4986G=	XP_016874579.1:p.Thr1662=
NM_015335.5:c.4989G= MANE Select	NP_056150.1:p.Thr1663=