Canonical Allele Identifier: CA2065359594

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975489G= , CM000674.2:g.115975489G=	GRCh38
NC_000012.11:g.116413294G= , CM000674.1:g.116413294G=	GRCh37
NC_000012.10:g.114897677G=	NCBI36
NG_023366.1:g.306698C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5588+26C= MANE Select	ENSP00000281928.3:n.5588+26C=
ENST00000548694.2:n.403C=
ENST00000648379.1:n.3956+26C=
ENST00000648737.1:n.5352+26C=
ENST00000648825.1:n.3773+26C=
ENST00000648916.1:n.3599+26C=
ENST00000649607.1:c.3772+26C=
ENST00000649775.1:c.2077+26C=
ENST00000650226.1:c.5588+26C=	ENSP00000496981.1:n.5588+26C=
ENST00000281928.7:c.5588+26C=	ENSP00000281928.3:n.5588+26C=
ENST00000548694.1:n.403C=
ENST00000552447.1:c.165+26C=
NM_015335.4:c.5588+26C=	NP_056150.1:n.5588+26C=
XM_011538080.1:c.5588+26C=	XP_011536382.1:n.5588+26C=
XM_011538081.1:c.5585+26C=	XP_011536383.1:n.5585+26C=
XM_011538082.1:c.5558+26C=	XP_011536384.1:n.5558+26C=
XM_011538080.2:c.5588+26C=	XP_011536382.1:n.5588+26C=
XM_011538081.2:c.5585+26C=	XP_011536383.1:n.5585+26C=
XM_011538082.2:c.5558+26C=	XP_011536384.1:n.5558+26C=
XM_017019090.1:c.5585+26C=	XP_016874579.1:n.5585+26C=
NM_015335.5:c.5588+26C= MANE Select	NP_056150.1:n.5588+26C=