Canonical Allele Identifier: CA2065386507
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115991686G= , CM000674.2:g.115991686G= GRCh38
NC_000012.11:g.116429491G= , CM000674.1:g.116429491G= GRCh37
NC_000012.10:g.114913874G= NCBI36
NG_023366.1:g.290501C=

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.3268C= MANE Select ENSP00000281928.3:p.Arg1090=
ENST00000548743.2:c.3238C= ENSP00000448553.2:p.Arg1080=
ENST00000549786.2:c.2696C=
ENST00000648379.1:n.1636C=
ENST00000648737.1:n.3032C=
ENST00000648825.1:n.8C=
ENST00000648916.1:n.1279C=
ENST00000649607.1:c.1452C=
ENST00000650226.1:c.3268C= ENSP00000496981.1:p.Arg1090=
ENST00000281928.7:c.3268C= ENSP00000281928.3:p.Arg1090=
NM_015335.4:c.3268C= NP_056150.1:p.Arg1090=
XM_011538080.1:c.3268C= XP_011536382.1:p.Arg1090=
XM_011538081.1:c.3265C= XP_011536383.1:p.Arg1089=
XM_011538082.1:c.3238C= XP_011536384.1:p.Arg1080=
XM_011538080.2:c.3268C= XP_011536382.1:p.Arg1090=
XM_011538081.2:c.3265C= XP_011536383.1:p.Arg1089=
XM_011538082.2:c.3238C= XP_011536384.1:p.Arg1080=
XM_017019090.1:c.3265C= XP_016874579.1:p.Arg1089=
NM_015335.5:c.3268C= MANE Select NP_056150.1:p.Arg1090=