Canonical Allele Identifier: CA2065371173
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115982358_115982427delinsTAAATAATAAACTTGCAAACAGTAACCTGGAGAATGAAAGAATTTCTCATATGCTCAGGTAAATTATCCA , CM000674.2:g.115982358_115982427delinsTAAATAATAAACTTGCAAACAGTAACCTGGAGAATGAAAGAATTTCTCATATGCTCAGGTAAATTATCCA GRCh38
NC_000012.11:g.116420163_116420232delinsTAAATAATAAACTTGCAAACAGTAACCTGGAGAATGAAAGAATTTCTCATATGCTCAGGTAAATTATCCA , CM000674.1:g.116420163_116420232delinsTAAATAATAAACTTGCAAACAGTAACCTGGAGAATGAAAGAATTTCTCATATGCTCAGGTAAATTATCCA GRCh37
NC_000012.10:g.114904546_114904615delinsTAAATAATAAACTTGCAAACAGTAACCTGGAGAATGAAAGAATTTCTCATATGCTCAGGTAAATTATCCA NCBI36
NG_023366.1:g.299760_299829delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.5132_5175+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000549786.2:c.4560_4629delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000648379.1:n.3500_3543+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000648737.1:n.4896_4939+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000648825.1:n.1872_1941delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000648916.1:n.3143_3186+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000649146.1:n.2375_2444delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000649607.1:c.3316_3359+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000649775.1:c.1621_1664+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000650226.1:c.5132_5175+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000281928.7:c.5132_5175+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000549786.1:c.496_565delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
ENST00000552340.1:c.164_207+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
NM_015335.4:c.5132_5175+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
XM_011538080.1:c.5132_5175+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
XM_011538081.1:c.5129_5172+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
XM_011538082.1:c.5102_5145+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
XM_011538080.2:c.5132_5175+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
XM_011538081.2:c.5129_5172+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
XM_011538082.2:c.5102_5145+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
XM_017019090.1:c.5129_5172+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA
NM_015335.5:c.5132_5175+26delinsTGGATAATTTACCTGAGCATATGAGAAATTCTTTCATTCTCCAGGTTACTGTTTGCAAGTTTATTATTTA