Canonical Allele Identifier: CA2065359650

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975518T= , CM000674.2:g.115975518T=	GRCh38
NC_000012.11:g.116413323T= , CM000674.1:g.116413323T=	GRCh37
NC_000012.10:g.114897706T=	NCBI36
NG_023366.1:g.306669A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5585A= MANE Select	ENSP00000281928.3:p.Asn1862=
ENST00000548694.2:n.374A=
ENST00000648379.1:n.3953A=
ENST00000648737.1:n.5349A=
ENST00000648825.1:n.3770A=
ENST00000648916.1:n.3596A=
ENST00000649607.1:c.3769A=
ENST00000649775.1:c.2074A=
ENST00000650226.1:c.5585A=	ENSP00000496981.1:p.Asn1862=
ENST00000281928.7:c.5585A=	ENSP00000281928.3:p.Asn1862=
ENST00000548694.1:n.374A=
ENST00000552447.1:c.162A=
NM_015335.4:c.5585A=	NP_056150.1:p.Asn1862=
XM_011538080.1:c.5585A=	XP_011536382.1:p.Asn1862=
XM_011538081.1:c.5582A=	XP_011536383.1:p.Asn1861=
XM_011538082.1:c.5555A=	XP_011536384.1:p.Asn1852=
XM_011538080.2:c.5585A=	XP_011536382.1:p.Asn1862=
XM_011538081.2:c.5582A=	XP_011536383.1:p.Asn1861=
XM_011538082.2:c.5555A=	XP_011536384.1:p.Asn1852=
XM_017019090.1:c.5582A=	XP_016874579.1:p.Asn1861=
NM_015335.5:c.5585A= MANE Select	NP_056150.1:p.Asn1862=