Canonical Allele Identifier: CA2065396900
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115997210T= , CM000674.2:g.115997210T= GRCh38
NC_000012.11:g.116435015T= , CM000674.1:g.116435015T= GRCh37
NC_000012.10:g.114919398T= NCBI36
NG_023366.1:g.284977A=

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.2590A= MANE Select ENSP00000281928.3:p.Met864=
ENST00000548743.2:c.2560A= ENSP00000448553.2:p.Met854=
ENST00000549786.2:c.2018A=
ENST00000647927.1:n.2963A=
ENST00000648173.1:n.1385A=
ENST00000648379.1:n.958A=
ENST00000648737.1:n.2354A=
ENST00000648916.1:n.601A=
ENST00000649607.1:c.774A=
ENST00000650226.1:c.2590A= ENSP00000496981.1:p.Met864=
ENST00000281928.7:c.2590A= ENSP00000281928.3:p.Met864=
NM_015335.4:c.2590A= NP_056150.1:p.Met864=
XM_011538080.1:c.2590A= XP_011536382.1:p.Met864=
XM_011538081.1:c.2587A= XP_011536383.1:p.Met863=
XM_011538082.1:c.2560A= XP_011536384.1:p.Met854=
XM_011538080.2:c.2590A= XP_011536382.1:p.Met864=
XM_011538081.2:c.2587A= XP_011536383.1:p.Met863=
XM_011538082.2:c.2560A= XP_011536384.1:p.Met854=
XM_017019090.1:c.2587A= XP_016874579.1:p.Met863=
NM_015335.5:c.2590A= MANE Select NP_056150.1:p.Met864=