Canonical Allele Identifier: CA2065386878

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991845C= , CM000674.2:g.115991845C=	GRCh38
NC_000012.11:g.116429650C= , CM000674.1:g.116429650C=	GRCh37
NC_000012.10:g.114914033C=	NCBI36
NG_023366.1:g.290342G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3109G= MANE Select	ENSP00000281928.3:p.Val1037=
ENST00000548743.2:c.3079G=	ENSP00000448553.2:p.Val1027=
ENST00000549786.2:c.2537G=
ENST00000648173.1:n.1904G=
ENST00000648379.1:n.1477G=
ENST00000648737.1:n.2873G=
ENST00000648916.1:n.1120G=
ENST00000649607.1:c.1293G=
ENST00000650226.1:c.3109G=	ENSP00000496981.1:p.Val1037=
ENST00000281928.7:c.3109G=	ENSP00000281928.3:p.Val1037=
NM_015335.4:c.3109G=	NP_056150.1:p.Val1037=
XM_011538080.1:c.3109G=	XP_011536382.1:p.Val1037=
XM_011538081.1:c.3106G=	XP_011536383.1:p.Val1036=
XM_011538082.1:c.3079G=	XP_011536384.1:p.Val1027=
XM_011538080.2:c.3109G=	XP_011536382.1:p.Val1037=
XM_011538081.2:c.3106G=	XP_011536383.1:p.Val1036=
XM_011538082.2:c.3079G=	XP_011536384.1:p.Val1027=
XM_017019090.1:c.3106G=	XP_016874579.1:p.Val1036=
NM_015335.5:c.3109G= MANE Select	NP_056150.1:p.Val1037=