Canonical Allele Identifier: CA2065371659

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982530C= , CM000674.2:g.115982530C=	GRCh38
NC_000012.11:g.116420335C= , CM000674.1:g.116420335C=	GRCh37
NC_000012.10:g.114904718C=	NCBI36
NG_023366.1:g.299657G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5029G= MANE Select	ENSP00000281928.3:p.Val1677=
ENST00000549786.2:c.4457G=
ENST00000648379.1:n.3397G=
ENST00000648737.1:n.4793G=
ENST00000648825.1:n.1769G=
ENST00000648916.1:n.3040G=
ENST00000649146.1:n.2272G=
ENST00000649607.1:c.3213G=
ENST00000649775.1:c.1518G=
ENST00000650226.1:c.5029G=	ENSP00000496981.1:p.Val1677=
ENST00000281928.7:c.5029G=	ENSP00000281928.3:p.Val1677=
ENST00000549786.1:c.393G=
ENST00000552340.1:c.61G=	ENSP00000449876.1:p.Val21=
NM_015335.4:c.5029G=	NP_056150.1:p.Val1677=
XM_011538080.1:c.5029G=	XP_011536382.1:p.Val1677=
XM_011538081.1:c.5026G=	XP_011536383.1:p.Val1676=
XM_011538082.1:c.4999G=	XP_011536384.1:p.Val1667=
XM_011538080.2:c.5029G=	XP_011536382.1:p.Val1677=
XM_011538081.2:c.5026G=	XP_011536383.1:p.Val1676=
XM_011538082.2:c.4999G=	XP_011536384.1:p.Val1667=
XM_017019090.1:c.5026G=	XP_016874579.1:p.Val1676=
NM_015335.5:c.5029G= MANE Select	NP_056150.1:p.Val1677=