Canonical Allele Identifier: CA2065398782
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.116022571A= , CM000674.2:g.116022571A= GRCh38
NC_000012.11:g.116460376A= , CM000674.1:g.116460376A= GRCh37
NC_000012.10:g.114944759A= NCBI36
NG_023366.1:g.259616T=

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.510T= MANE Select ENSP00000281928.3:p.Phe170=
ENST00000548743.2:c.480T= ENSP00000448553.2:p.Phe160=
ENST00000647567.1:c.420T= ENSP00000497136.1:p.Phe140=
ENST00000648737.1:n.274T=
ENST00000650226.1:c.510T= ENSP00000496981.1:p.Phe170=
ENST00000281928.7:c.510T= ENSP00000281928.3:p.Phe170=
NM_015335.4:c.510T= NP_056150.1:p.Phe170=
XM_011538080.1:c.510T= XP_011536382.1:p.Phe170=
XM_011538081.1:c.510T= XP_011536383.1:p.Phe170=
XM_011538082.1:c.480T= XP_011536384.1:p.Phe160=
XM_011538080.2:c.510T= XP_011536382.1:p.Phe170=
XM_011538081.2:c.510T= XP_011536383.1:p.Phe170=
XM_011538082.2:c.480T= XP_011536384.1:p.Phe160=
XM_017019090.1:c.510T= XP_016874579.1:p.Phe170=
NM_015335.5:c.510T= MANE Select NP_056150.1:p.Phe170=