Canonical Allele Identifier: CA2065386894

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991859T= , CM000674.2:g.115991859T=	GRCh38
NC_000012.11:g.116429664T= , CM000674.1:g.116429664T=	GRCh37
NC_000012.10:g.114914047T=	NCBI36
NG_023366.1:g.290328A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3095A= MANE Select	ENSP00000281928.3:p.Asn1032=
ENST00000548743.2:c.3065A=	ENSP00000448553.2:p.Asn1022=
ENST00000549786.2:c.2523A=
ENST00000648173.1:n.1890A=
ENST00000648379.1:n.1463A=
ENST00000648737.1:n.2859A=
ENST00000648916.1:n.1106A=
ENST00000649607.1:c.1279A=
ENST00000650226.1:c.3095A=	ENSP00000496981.1:p.Asn1032=
ENST00000281928.7:c.3095A=	ENSP00000281928.3:p.Asn1032=
NM_015335.4:c.3095A=	NP_056150.1:p.Asn1032=
XM_011538080.1:c.3095A=	XP_011536382.1:p.Asn1032=
XM_011538081.1:c.3092A=	XP_011536383.1:p.Asn1031=
XM_011538082.1:c.3065A=	XP_011536384.1:p.Asn1022=
XM_011538080.2:c.3095A=	XP_011536382.1:p.Asn1032=
XM_011538081.2:c.3092A=	XP_011536383.1:p.Asn1031=
XM_011538082.2:c.3065A=	XP_011536384.1:p.Asn1022=
XM_017019090.1:c.3092A=	XP_016874579.1:p.Asn1031=
NM_015335.5:c.3095A= MANE Select	NP_056150.1:p.Asn1032=