HGVS | Genome Assembly |
---|---|
NC_000009.12:g.6587164_6587174del , CM000671.2:g.6587164_6587174del | GRCh38 |
NC_000009.11:g.6587164_6587174del , CM000671.1:g.6587164_6587174del | GRCh37 |
NC_000009.10:g.6577164_6577174del | NCBI36 |
NG_016397.1:g.63524_63534del , LRG_643:g.63524_63534del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321612.8:c.1822_1832del MANE Select | ENSP00000370737.4:p.Tyr608LeufsTer? | |
ENST00000639364.1:n.1522_1532del | ||
ENST00000639443.1:n.1390_1400del | ||
ENST00000639954.1:n.1530_1540del | ||
ENST00000640592.1:n.1705_1715del | ||
ENST00000321612.6:c.1822_1832del | ENSP00000370737.3:p.Tyr608LeufsTer? | |
NM_000170.2:c.1822_1832del , LRG_643t1:c.1822_1832del | NP_000161.2:p.Tyr608LeufsTer? | |
NM_000170.3:c.1822_1832del MANE Select | NP_000161.2:p.Tyr608LeufsTer? |