Canonical Allele Identifier: CA2065381476
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.116012803C= , CM000674.2:g.116012803C= GRCh38
NC_000012.11:g.116450608C= , CM000674.1:g.116450608C= GRCh37
NC_000012.10:g.114934991C= NCBI36
NG_023366.1:g.269384G=

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.1274G= MANE Select ENSP00000281928.3:p.Cys425=
ENST00000548743.2:c.1244G= ENSP00000448553.2:p.Cys415=
ENST00000549786.2:c.702G=
ENST00000647567.1:c.1181G= ENSP00000497136.1:p.Cys394=
ENST00000648737.1:n.1038G=
ENST00000650226.1:c.1274G= ENSP00000496981.1:p.Cys425=
ENST00000281928.7:c.1274G= ENSP00000281928.3:p.Cys425=
NM_015335.4:c.1274G= NP_056150.1:p.Cys425=
XM_011538080.1:c.1274G= XP_011536382.1:p.Cys425=
XM_011538081.1:c.1274G= XP_011536383.1:p.Cys425=
XM_011538082.1:c.1244G= XP_011536384.1:p.Cys415=
XM_011538080.2:c.1274G= XP_011536382.1:p.Cys425=
XM_011538081.2:c.1274G= XP_011536383.1:p.Cys425=
XM_011538082.2:c.1244G= XP_011536384.1:p.Cys415=
XM_017019090.1:c.1274G= XP_016874579.1:p.Cys425=
NM_015335.5:c.1274G= MANE Select NP_056150.1:p.Cys425=