HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152304545_152304568del , CM000663.2:g.152304545_152304568del | GRCh38 |
NC_000001.10:g.152277021_152277044del , CM000663.1:g.152277021_152277044del | GRCh37 |
NC_000001.9:g.150543645_150543668del | NCBI36 |
NG_016190.1:g.25638_25661del , LRG_1028:g.25638_25661del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368799.2:c.10320_10343del MANE Select | ENSP00000357789.1:p.Ser3441_Ser3448del | |
ENST00000368799.1:c.10320_10343del | ENSP00000357789.1:p.Ser3441_Ser3448del | |
NM_002016.1:c.10320_10343del , LRG_1028t1:c.10320_10343del | NP_002007.1:p.Ser3441_Ser3448del | |
XM_011509329.1:c.9109-733_9109-710del | XP_011507631.1:n.9109-733_9109-710del | |
NM_002016.2:c.10320_10343del MANE Select | NP_002007.1:p.Ser3441_Ser3448del |