Canonical Allele Identifier: CA2065396935
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115997219A= , CM000674.2:g.115997219A= GRCh38
NC_000012.11:g.116435024A= , CM000674.1:g.116435024A= GRCh37
NC_000012.10:g.114919407A= NCBI36
NG_023366.1:g.284968T=

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.2581T= MANE Select ENSP00000281928.3:p.Leu861=
ENST00000548743.2:c.2551T= ENSP00000448553.2:p.Leu851=
ENST00000549786.2:c.2009T=
ENST00000647927.1:n.2954T=
ENST00000648173.1:n.1376T=
ENST00000648379.1:n.949T=
ENST00000648737.1:n.2345T=
ENST00000648916.1:n.592T=
ENST00000649607.1:c.765T=
ENST00000650226.1:c.2581T= ENSP00000496981.1:p.Leu861=
ENST00000281928.7:c.2581T= ENSP00000281928.3:p.Leu861=
NM_015335.4:c.2581T= NP_056150.1:p.Leu861=
XM_011538080.1:c.2581T= XP_011536382.1:p.Leu861=
XM_011538081.1:c.2578T= XP_011536383.1:p.Leu860=
XM_011538082.1:c.2551T= XP_011536384.1:p.Leu851=
XM_011538080.2:c.2581T= XP_011536382.1:p.Leu861=
XM_011538081.2:c.2578T= XP_011536383.1:p.Leu860=
XM_011538082.2:c.2551T= XP_011536384.1:p.Leu851=
XM_017019090.1:c.2578T= XP_016874579.1:p.Leu860=
NM_015335.5:c.2581T= MANE Select NP_056150.1:p.Leu861=