HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21010525_21010530del , CM000664.2:g.21010525_21010530del | GRCh38 |
NC_000002.11:g.21233397_21233402del , CM000664.1:g.21233397_21233402del | GRCh37 |
NC_000002.10:g.21086902_21086907del | NCBI36 |
NG_011793.1:g.38544_38549del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233242.5:c.6338_6343del MANE Select | ENSP00000233242.1:p.Ala2113_Leu2115delinsVal | |
ENST00000616098.4:c.6338_6343del | ENSP00000477990.1:p.Ala2113_Leu2115delinsVal | |
NM_000384.2:c.6338_6343del | NP_000375.2:p.Ala2113_Leu2115delinsVal | |
XM_011532809.1:c.5869+203_5869+208del | XP_011531111.1:n.5869+203_5869+208del | |
NM_000384.3:c.6338_6343del MANE Select | NP_000375.3:p.Ala2113_Leu2115delinsVal |