Canonical Allele Identifier: CA2065398777
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.116022566T= , CM000674.2:g.116022566T= GRCh38
NC_000012.11:g.116460371T= , CM000674.1:g.116460371T= GRCh37
NC_000012.10:g.114944754T= NCBI36
NG_023366.1:g.259621A=

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.515A= MANE Select ENSP00000281928.3:p.His172=
ENST00000548743.2:c.485A= ENSP00000448553.2:p.His162=
ENST00000647567.1:c.425A= ENSP00000497136.1:p.His142=
ENST00000648737.1:n.279A=
ENST00000650226.1:c.515A= ENSP00000496981.1:p.His172=
ENST00000281928.7:c.515A= ENSP00000281928.3:p.His172=
NM_015335.4:c.515A= NP_056150.1:p.His172=
XM_011538080.1:c.515A= XP_011536382.1:p.His172=
XM_011538081.1:c.515A= XP_011536383.1:p.His172=
XM_011538082.1:c.485A= XP_011536384.1:p.His162=
XM_011538080.2:c.515A= XP_011536382.1:p.His172=
XM_011538081.2:c.515A= XP_011536383.1:p.His172=
XM_011538082.2:c.485A= XP_011536384.1:p.His162=
XM_017019090.1:c.515A= XP_016874579.1:p.His172=
NM_015335.5:c.515A= MANE Select NP_056150.1:p.His172=