Canonical Allele Identifier: CA2065371511

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982475G= , CM000674.2:g.115982475G=	GRCh38
NC_000012.11:g.116420280G= , CM000674.1:g.116420280G=	GRCh37
NC_000012.10:g.114904663G=	NCBI36
NG_023366.1:g.299712C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5084C= MANE Select	ENSP00000281928.3:p.Ser1695=
ENST00000549786.2:c.4512C=
ENST00000648379.1:n.3452C=
ENST00000648737.1:n.4848C=
ENST00000648825.1:n.1824C=
ENST00000648916.1:n.3095C=
ENST00000649146.1:n.2327C=
ENST00000649607.1:c.3268C=
ENST00000649775.1:c.1573C=
ENST00000650226.1:c.5084C=	ENSP00000496981.1:p.Ser1695=
ENST00000281928.7:c.5084C=	ENSP00000281928.3:p.Ser1695=
ENST00000549786.1:c.448C=
ENST00000552340.1:c.116C=	ENSP00000449876.1:p.Ser39=
NM_015335.4:c.5084C=	NP_056150.1:p.Ser1695=
XM_011538080.1:c.5084C=	XP_011536382.1:p.Ser1695=
XM_011538081.1:c.5081C=	XP_011536383.1:p.Ser1694=
XM_011538082.1:c.5054C=	XP_011536384.1:p.Ser1685=
XM_011538080.2:c.5084C=	XP_011536382.1:p.Ser1695=
XM_011538081.2:c.5081C=	XP_011536383.1:p.Ser1694=
XM_011538082.2:c.5054C=	XP_011536384.1:p.Ser1685=
XM_017019090.1:c.5081C=	XP_016874579.1:p.Ser1694=
NM_015335.5:c.5084C= MANE Select	NP_056150.1:p.Ser1695=