Canonical Allele Identifier: CA386881091

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420237T>G (hg19) ; chr12:g.115982432T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982432T>G , CM000674.2:g.115982432T>G	GRCh38
NC_000012.11:g.116420237T>G , CM000674.1:g.116420237T>G	GRCh37
NC_000012.10:g.114904620T>G	NCBI36
NG_023366.1:g.299755A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5127A>C MANE Select	ENSP00000281928.3:p.Glu1709Asp
ENST00000549786.2:c.4555A>C
ENST00000648379.1:n.3495A>C
ENST00000648737.1:n.4891A>C
ENST00000648825.1:n.1867A>C
ENST00000648916.1:n.3138A>C
ENST00000649146.1:n.2370A>C
ENST00000649607.1:c.3311A>C
ENST00000649775.1:c.1616A>C
ENST00000650226.1:c.5127A>C	ENSP00000496981.1:p.Glu1709Asp
ENST00000281928.7:c.5127A>C	ENSP00000281928.3:p.Glu1709Asp
ENST00000549786.1:c.491A>C
ENST00000552340.1:c.159A>C	ENSP00000449876.1:p.Glu53Asp
NM_015335.4:c.5127A>C	NP_056150.1:p.Glu1709Asp
XM_011538080.1:c.5127A>C	XP_011536382.1:p.Glu1709Asp
XM_011538081.1:c.5124A>C	XP_011536383.1:p.Glu1708Asp
XM_011538082.1:c.5097A>C	XP_011536384.1:p.Glu1699Asp
XM_011538080.2:c.5127A>C	XP_011536382.1:p.Glu1709Asp
XM_011538081.2:c.5124A>C	XP_011536383.1:p.Glu1708Asp
XM_011538082.2:c.5097A>C	XP_011536384.1:p.Glu1699Asp
XM_017019090.1:c.5124A>C	XP_016874579.1:p.Glu1708Asp
NM_015335.5:c.5127A>C MANE Select	NP_056150.1:p.Glu1709Asp