HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085840_186085843delinsATTT , CM000666.2:g.186085840_186085843delinsATTT | GRCh38 |
NC_000004.11:g.187006994_187006997delinsATTT , CM000666.1:g.187006994_187006997delinsATTT | GRCh37 |
NC_000004.10:g.187243988_187243991delinsATTT | NCBI36 |
NG_007278.1:g.21686_21689delinsATTT , LRG_117:g.21686_21689delinsATTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3234_*3237delinsATTT | ENSP00000513675.1:n.*3234_*3237delinsATTT | |
ENST00000698353.1:n.3557_3560delinsATTT | ||
ENST00000698354.1:c.*967_*970delinsATTT | ENSP00000513676.1:n.*967_*970delinsATTT | |
ENST00000296795.8:c.*967_*970delinsATTT MANE Select | ENSP00000296795.3:n.*967_*970delinsATTT | |
ENST00000296795.7:c.*967_*970delinsATTT | ENSP00000296795.2:n.*967_*970delinsATTT | |
NM_003265.3:c.*967_*970delinsATTT MANE Select | NP_003256.1:n.*967_*970delinsATTT |