Canonical Allele Identifier: CA2065371494

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982469T= , CM000674.2:g.115982469T=	GRCh38
NC_000012.11:g.116420274T= , CM000674.1:g.116420274T=	GRCh37
NC_000012.10:g.114904657T=	NCBI36
NG_023366.1:g.299718A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5090A= MANE Select	ENSP00000281928.3:p.Asn1697=
ENST00000549786.2:c.4518A=
ENST00000648379.1:n.3458A=
ENST00000648737.1:n.4854A=
ENST00000648825.1:n.1830A=
ENST00000648916.1:n.3101A=
ENST00000649146.1:n.2333A=
ENST00000649607.1:c.3274A=
ENST00000649775.1:c.1579A=
ENST00000650226.1:c.5090A=	ENSP00000496981.1:p.Asn1697=
ENST00000281928.7:c.5090A=	ENSP00000281928.3:p.Asn1697=
ENST00000549786.1:c.454A=
ENST00000552340.1:c.122A=	ENSP00000449876.1:p.Asn41=
NM_015335.4:c.5090A=	NP_056150.1:p.Asn1697=
XM_011538080.1:c.5090A=	XP_011536382.1:p.Asn1697=
XM_011538081.1:c.5087A=	XP_011536383.1:p.Asn1696=
XM_011538082.1:c.5060A=	XP_011536384.1:p.Asn1687=
XM_011538080.2:c.5090A=	XP_011536382.1:p.Asn1697=
XM_011538081.2:c.5087A=	XP_011536383.1:p.Asn1696=
XM_011538082.2:c.5060A=	XP_011536384.1:p.Asn1687=
XM_017019090.1:c.5087A=	XP_016874579.1:p.Asn1696=
NM_015335.5:c.5090A= MANE Select	NP_056150.1:p.Asn1697=