Canonical Allele Identifier: CA2065371902
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115982607G= , CM000674.2:g.115982607G= GRCh38
NC_000012.11:g.116420412G= , CM000674.1:g.116420412G= GRCh37
NC_000012.10:g.114904795G= NCBI36
NG_023366.1:g.299580C=

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.4956-4C= MANE Select ENSP00000281928.3:n.4956-4C=
ENST00000549786.2:c.4384-4C=
ENST00000648379.1:n.3324-4C=
ENST00000648737.1:n.4720-4C=
ENST00000648825.1:n.1696-4C=
ENST00000648916.1:n.2967-4C=
ENST00000649146.1:n.2195C=
ENST00000649607.1:c.3140-4C=
ENST00000649775.1:c.1453-12C=
ENST00000650226.1:c.4956-4C= ENSP00000496981.1:n.4956-4C=
ENST00000281928.7:c.4956-4C= ENSP00000281928.3:n.4956-4C=
ENST00000549786.1:c.320-4C=
NM_015335.4:c.4956-4C= NP_056150.1:n.4956-4C=
XM_011538080.1:c.4956-4C= XP_011536382.1:n.4956-4C=
XM_011538081.1:c.4953-4C= XP_011536383.1:n.4953-4C=
XM_011538082.1:c.4926-4C= XP_011536384.1:n.4926-4C=
XM_011538080.2:c.4956-4C= XP_011536382.1:n.4956-4C=
XM_011538081.2:c.4953-4C= XP_011536383.1:n.4953-4C=
XM_011538082.2:c.4926-4C= XP_011536384.1:n.4926-4C=
XM_017019090.1:c.4953-4C= XP_016874579.1:n.4953-4C=
NM_015335.5:c.4956-4C= MANE Select NP_056150.1:n.4956-4C=