HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20189211_20189212delinsTG , CM000675.2:g.20189211_20189212delinsTG | GRCh38 |
NC_000013.10:g.20763350_20763351delinsTG , CM000675.1:g.20763350_20763351delinsTG | GRCh37 |
NC_000013.9:g.19661350_19661351delinsTG | NCBI36 |
NG_008358.1:g.8764_8765delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.370_371delinsCA | ENSP00000372295.1:p.Gln124= | |
ENST00000382848.5:c.370_371delinsCA MANE Select | ENSP00000372299.4:p.Gln124= | |
ENST00000382844.1:c.370_371delinsCA | ENSP00000372295.1:p.Gln124= | |
ENST00000382848.4:c.370_371delinsCA | ENSP00000372299.4:p.Gln124= | |
NM_004004.5:c.370_371delinsCA | NP_003995.2:p.Gln124= | |
XM_011535049.1:c.370_371delinsCA | XP_011533351.1:p.Gln124= | |
XM_011535049.2:c.370_371delinsCA | XP_011533351.1:p.Gln124= | |
NM_004004.6:c.370_371delinsCA MANE Select | NP_003995.2:p.Gln124= |