Canonical Allele Identifier: CA2065386371

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991657G= , CM000674.2:g.115991657G=	GRCh38
NC_000012.11:g.116429462G= , CM000674.1:g.116429462G=	GRCh37
NC_000012.10:g.114913845G=	NCBI36
NG_023366.1:g.290530C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3297C= MANE Select	ENSP00000281928.3:p.Thr1099=
ENST00000549786.2:c.2725C=
ENST00000648379.1:n.1665C=
ENST00000648737.1:n.3061C=
ENST00000648825.1:n.37C=
ENST00000648916.1:n.1308C=
ENST00000649607.1:c.1481C=
ENST00000650226.1:c.3297C=	ENSP00000496981.1:p.Thr1099=
ENST00000281928.7:c.3297C=	ENSP00000281928.3:p.Thr1099=
NM_015335.4:c.3297C=	NP_056150.1:p.Thr1099=
XM_011538080.1:c.3297C=	XP_011536382.1:p.Thr1099=
XM_011538081.1:c.3294C=	XP_011536383.1:p.Thr1098=
XM_011538082.1:c.3267C=	XP_011536384.1:p.Thr1089=
XM_011538080.2:c.3297C=	XP_011536382.1:p.Thr1099=
XM_011538081.2:c.3294C=	XP_011536383.1:p.Thr1098=
XM_011538082.2:c.3267C=	XP_011536384.1:p.Thr1089=
XM_017019090.1:c.3294C=	XP_016874579.1:p.Thr1098=
NM_015335.5:c.3297C= MANE Select	NP_056150.1:p.Thr1099=