HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91055982_91055983delinsAT , CM000674.2:g.91055982_91055983delinsAT | GRCh38 |
NC_000012.11:g.91449759_91449760delinsAT , CM000674.1:g.91449759_91449760delinsAT | GRCh37 |
NC_000012.10:g.89973890_89973891delinsAT | NCBI36 |
NG_021223.1:g.7372_7373delinsAT , LRG_538:g.7372_7373delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266719.4:c.299_300delinsAT MANE Select | ENSP00000266719.3:p.Ile100Asn | |
ENST00000266719.3:c.299_300delinsAT | ENSP00000266719.3:p.Ile100Asn | |
NM_007035.3:c.299_300delinsAT , LRG_538t1:c.299_300delinsAT | NP_008966.1:p.Ile100Asn | |
XM_011537781.1:c.299_300delinsAT | XP_011536083.1:p.Ile100Asn | |
NM_007035.4:c.299_300delinsAT MANE Select | NP_008966.1:p.Ile100Asn |