Canonical Allele Identifier: CA2065386771

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991795G= , CM000674.2:g.115991795G=	GRCh38
NC_000012.11:g.116429600G= , CM000674.1:g.116429600G=	GRCh37
NC_000012.10:g.114913983G=	NCBI36
NG_023366.1:g.290392C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3159C= MANE Select	ENSP00000281928.3:p.Thr1053=
ENST00000548743.2:c.3129C=	ENSP00000448553.2:p.Thr1043=
ENST00000549786.2:c.2587C=
ENST00000648173.1:n.1954C=
ENST00000648379.1:n.1527C=
ENST00000648737.1:n.2923C=
ENST00000648916.1:n.1170C=
ENST00000649607.1:c.1343C=
ENST00000650226.1:c.3159C=	ENSP00000496981.1:p.Thr1053=
ENST00000281928.7:c.3159C=	ENSP00000281928.3:p.Thr1053=
NM_015335.4:c.3159C=	NP_056150.1:p.Thr1053=
XM_011538080.1:c.3159C=	XP_011536382.1:p.Thr1053=
XM_011538081.1:c.3156C=	XP_011536383.1:p.Thr1052=
XM_011538082.1:c.3129C=	XP_011536384.1:p.Thr1043=
XM_011538080.2:c.3159C=	XP_011536382.1:p.Thr1053=
XM_011538081.2:c.3156C=	XP_011536383.1:p.Thr1052=
XM_011538082.2:c.3129C=	XP_011536384.1:p.Thr1043=
XM_017019090.1:c.3156C=	XP_016874579.1:p.Thr1052=
NM_015335.5:c.3159C= MANE Select	NP_056150.1:p.Thr1053=