Canonical Allele Identifier: CA2065381463
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.116012799G= , CM000674.2:g.116012799G= GRCh38
NC_000012.11:g.116450604G= , CM000674.1:g.116450604G= GRCh37
NC_000012.10:g.114934987G= NCBI36
NG_023366.1:g.269388C=

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.1278C= MANE Select ENSP00000281928.3:p.Ser426=
ENST00000548743.2:c.1248C= ENSP00000448553.2:p.Ser416=
ENST00000549786.2:c.706C=
ENST00000647567.1:c.1185C= ENSP00000497136.1:p.Ser395=
ENST00000648737.1:n.1042C=
ENST00000650226.1:c.1278C= ENSP00000496981.1:p.Ser426=
ENST00000281928.7:c.1278C= ENSP00000281928.3:p.Ser426=
NM_015335.4:c.1278C= NP_056150.1:p.Ser426=
XM_011538080.1:c.1278C= XP_011536382.1:p.Ser426=
XM_011538081.1:c.1278C= XP_011536383.1:p.Ser426=
XM_011538082.1:c.1248C= XP_011536384.1:p.Ser416=
XM_011538080.2:c.1278C= XP_011536382.1:p.Ser426=
XM_011538081.2:c.1278C= XP_011536383.1:p.Ser426=
XM_011538082.2:c.1248C= XP_011536384.1:p.Ser416=
XM_017019090.1:c.1278C= XP_016874579.1:p.Ser426=
NM_015335.5:c.1278C= MANE Select NP_056150.1:p.Ser426=