Canonical Allele Identifier: CA2065396649
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115997086A= , CM000674.2:g.115997086A= GRCh38
NC_000012.11:g.116434891A= , CM000674.1:g.116434891A= GRCh37
NC_000012.10:g.114919274A= NCBI36
NG_023366.1:g.285101T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.2714T= MANE Select ENSP00000281928.3:p.Met905=
ENST00000548743.2:c.2684T= ENSP00000448553.2:p.Met895=
ENST00000549786.2:c.2142T=
ENST00000647927.1:n.3087T=
ENST00000648173.1:n.1509T=
ENST00000648379.1:n.1082T=
ENST00000648737.1:n.2478T=
ENST00000648916.1:n.725T=
ENST00000649607.1:c.898T=
ENST00000650226.1:c.2714T= ENSP00000496981.1:p.Met905=
ENST00000281928.7:c.2714T= ENSP00000281928.3:p.Met905=
NM_015335.4:c.2714T= NP_056150.1:p.Met905=
XM_011538080.1:c.2714T= XP_011536382.1:p.Met905=
XM_011538081.1:c.2711T= XP_011536383.1:p.Met904=
XM_011538082.1:c.2684T= XP_011536384.1:p.Met895=
XM_011538080.2:c.2714T= XP_011536382.1:p.Met905=
XM_011538081.2:c.2711T= XP_011536383.1:p.Met904=
XM_011538082.2:c.2684T= XP_011536384.1:p.Met895=
XM_017019090.1:c.2711T= XP_016874579.1:p.Met904=
NM_015335.5:c.2714T= MANE Select NP_056150.1:p.Met905=