HGVS | Genome Assembly |
---|---|
NC_000011.10:g.86954631_86954643delinsACGTTTTGGCTTC , CM000673.2:g.86954631_86954643delinsACGTTTTGGCTTC | GRCh38 |
NC_000011.9:g.86665673_86665685delinsACGTTTTGGCTTC , CM000673.1:g.86665673_86665685delinsACGTTTTGGCTTC | GRCh37 |
NC_000011.8:g.86343321_86343333delinsACGTTTTGGCTTC | NCBI36 |
NG_011752.1:g.5749_5761delinsGAAGCCAAAACGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000531380.2:c.285+158_285+170delinsGAAGCCAAAACGT MANE Select | ENSP00000434034.1:n.285+158_285+170delinsGAAGCCAAAACGT | |
ENST00000531380.1:c.285+158_285+170delinsGAAGCCAAAACGT | ENSP00000434034.1:n.285+158_285+170delinsGAAGCCAAAACGT | |
NM_012193.3:c.285+158_285+170delinsGAAGCCAAAACGT | NP_036325.2:n.285+158_285+170delinsGAAGCCAAAACGT | |
NM_012193.4:c.285+158_285+170delinsGAAGCCAAAACGT MANE Select | NP_036325.2:n.285+158_285+170delinsGAAGCCAAAACGT |