Canonical Allele Identifier: CA16619439
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 423638
ClinVar RCV Id: RCV000487114
dbSNP Id: rs1064796543

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115975314C>T , CM000674.2:g.115975314C>T GRCh38
NC_000012.11:g.116413119C>T , CM000674.1:g.116413119C>T GRCh37
NC_000012.10:g.114897502C>T NCBI36
NG_023366.1:g.306873G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.5589-1G>A MANE Select ENSP00000281928.3:n.5589-1G>A
ENST00000548694.2:n.578G>A
ENST00000648379.1:n.3957-1G>A
ENST00000648737.1:n.5353-1G>A
ENST00000648825.1:n.3774-1G>A
ENST00000648916.1:n.3600-1G>A
ENST00000649607.1:c.3773-1G>A
ENST00000649775.1:c.2078-1G>A
ENST00000650226.1:c.5624G>A ENSP00000496981.1:p.Arg1875Lys
ENST00000281928.7:c.5589-1G>A ENSP00000281928.3:n.5589-1G>A
ENST00000548694.1:n.578G>A
ENST00000552447.1:c.201G>A
NM_015335.4:c.5589-1G>A NP_056150.1:n.5589-1G>A
XM_011538080.1:c.5624G>A XP_011536382.1:p.Arg1875Lys
XM_011538081.1:c.5621G>A XP_011536383.1:p.Arg1874Lys
XM_011538082.1:c.5594G>A XP_011536384.1:p.Arg1865Lys
XM_011538080.2:c.5624G>A XP_011536382.1:p.Arg1875Lys
XM_011538081.2:c.5621G>A XP_011536383.1:p.Arg1874Lys
XM_011538082.2:c.5594G>A XP_011536384.1:p.Arg1865Lys
XM_017019090.1:c.5586-1G>A XP_016874579.1:n.5586-1G>A
NM_015335.5:c.5589-1G>A MANE Select NP_056150.1:n.5589-1G>A