Canonical Allele Identifier: CA2065387160
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115991955T= , CM000674.2:g.115991955T= GRCh38
NC_000012.11:g.116429760T= , CM000674.1:g.116429760T= GRCh37
NC_000012.10:g.114914143T= NCBI36
NG_023366.1:g.290232A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.2999A= MANE Select ENSP00000281928.3:p.Asn1000=
ENST00000548743.2:c.2969A= ENSP00000448553.2:p.Asn990=
ENST00000549786.2:c.2427A=
ENST00000648173.1:n.1794A=
ENST00000648379.1:n.1367A=
ENST00000648737.1:n.2763A=
ENST00000648916.1:n.1010A=
ENST00000649607.1:c.1183A=
ENST00000650226.1:c.2999A= ENSP00000496981.1:p.Asn1000=
ENST00000281928.7:c.2999A= ENSP00000281928.3:p.Asn1000=
NM_015335.4:c.2999A= NP_056150.1:p.Asn1000=
XM_011538080.1:c.2999A= XP_011536382.1:p.Asn1000=
XM_011538081.1:c.2996A= XP_011536383.1:p.Asn999=
XM_011538082.1:c.2969A= XP_011536384.1:p.Asn990=
XM_011538080.2:c.2999A= XP_011536382.1:p.Asn1000=
XM_011538081.2:c.2996A= XP_011536383.1:p.Asn999=
XM_011538082.2:c.2969A= XP_011536384.1:p.Asn990=
XM_017019090.1:c.2996A= XP_016874579.1:p.Asn999=
NM_015335.5:c.2999A= MANE Select NP_056150.1:p.Asn1000=