Canonical Allele Identifier: CA2065386498
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115991685C= , CM000674.2:g.115991685C= GRCh38
NC_000012.11:g.116429490C= , CM000674.1:g.116429490C= GRCh37
NC_000012.10:g.114913873C= NCBI36
NG_023366.1:g.290502G=

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.3269G= MANE Select ENSP00000281928.3:p.Arg1090=
ENST00000548743.2:c.3239G= ENSP00000448553.2:p.Arg1080=
ENST00000549786.2:c.2697G=
ENST00000648379.1:n.1637G=
ENST00000648737.1:n.3033G=
ENST00000648825.1:n.9G=
ENST00000648916.1:n.1280G=
ENST00000649607.1:c.1453G=
ENST00000650226.1:c.3269G= ENSP00000496981.1:p.Arg1090=
ENST00000281928.7:c.3269G= ENSP00000281928.3:p.Arg1090=
NM_015335.4:c.3269G= NP_056150.1:p.Arg1090=
XM_011538080.1:c.3269G= XP_011536382.1:p.Arg1090=
XM_011538081.1:c.3266G= XP_011536383.1:p.Arg1089=
XM_011538082.1:c.3239G= XP_011536384.1:p.Arg1080=
XM_011538080.2:c.3269G= XP_011536382.1:p.Arg1090=
XM_011538081.2:c.3266G= XP_011536383.1:p.Arg1089=
XM_011538082.2:c.3239G= XP_011536384.1:p.Arg1080=
XM_017019090.1:c.3266G= XP_016874579.1:p.Arg1089=
NM_015335.5:c.3269G= MANE Select NP_056150.1:p.Arg1090=