Canonical Allele Identifier: CA386881221

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420295T>A (hg19) ; chr12:g.115982490T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982490T>A , CM000674.2:g.115982490T>A	GRCh38
NC_000012.11:g.116420295T>A , CM000674.1:g.116420295T>A	GRCh37
NC_000012.10:g.114904678T>A	NCBI36
NG_023366.1:g.299697A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5069A>T MANE Select	ENSP00000281928.3:p.Glu1690Val
ENST00000549786.2:c.4497A>T
ENST00000648379.1:n.3437A>T
ENST00000648737.1:n.4833A>T
ENST00000648825.1:n.1809A>T
ENST00000648916.1:n.3080A>T
ENST00000649146.1:n.2312A>T
ENST00000649607.1:c.3253A>T
ENST00000649775.1:c.1558A>T
ENST00000650226.1:c.5069A>T	ENSP00000496981.1:p.Glu1690Val
ENST00000281928.7:c.5069A>T	ENSP00000281928.3:p.Glu1690Val
ENST00000549786.1:c.433A>T
ENST00000552340.1:c.101A>T	ENSP00000449876.1:p.Glu34Val
NM_015335.4:c.5069A>T	NP_056150.1:p.Glu1690Val
XM_011538080.1:c.5069A>T	XP_011536382.1:p.Glu1690Val
XM_011538081.1:c.5066A>T	XP_011536383.1:p.Glu1689Val
XM_011538082.1:c.5039A>T	XP_011536384.1:p.Glu1680Val
XM_011538080.2:c.5069A>T	XP_011536382.1:p.Glu1690Val
XM_011538081.2:c.5066A>T	XP_011536383.1:p.Glu1689Val
XM_011538082.2:c.5039A>T	XP_011536384.1:p.Glu1680Val
XM_017019090.1:c.5066A>T	XP_016874579.1:p.Glu1689Val
NM_015335.5:c.5069A>T MANE Select	NP_056150.1:p.Glu1690Val