HGVS | Genome Assembly |
---|---|
NC_000001.11:g.147908424_147908429del , CM000663.2:g.147908424_147908429del | GRCh38 |
NC_000001.10:g.147380551_147380556del , CM000663.1:g.147380551_147380556del | GRCh37 |
NC_000001.9:g.145847175_145847180del | NCBI36 |
NG_016242.1:g.10606_10611del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369235.2:c.469_474del MANE Select | ENSP00000358238.1:p.Phe157_Lys158del | |
ENST00000369235.1:c.469_474del | ENSP00000358238.1:p.Phe157_Lys158del | |
NM_005267.4:c.469_474del | NP_005258.2:p.Phe157_Lys158del | |
XM_011509416.1:c.469_474del | XP_011507718.1:p.Phe157_Lys158del | |
XM_011509417.1:c.469_474del | XP_011507719.1:p.Phe157_Lys158del | |
XM_011509417.2:c.469_474del | XP_011507719.1:p.Phe157_Lys158del | |
XR_002956281.1:n.1384_1389del | ||
NM_005267.5:c.469_474del MANE Select | NP_005258.2:p.Phe157_Lys158del |