HGVS | Genome Assembly |
---|---|
NC_000001.11:g.147908385_147908399del , CM000663.2:g.147908385_147908399del | GRCh38 |
NC_000001.10:g.147380512_147380526del , CM000663.1:g.147380512_147380526del | GRCh37 |
NC_000001.9:g.145847136_145847150del | NCBI36 |
NG_016242.1:g.10567_10581del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369235.2:c.430_444del MANE Select | ENSP00000358238.1:p.Glu144_Leu148del | |
ENST00000369235.1:c.430_444del | ENSP00000358238.1:p.Glu144_Leu148del | |
NM_005267.4:c.430_444del | NP_005258.2:p.Glu144_Leu148del | |
XM_011509416.1:c.430_444del | XP_011507718.1:p.Glu144_Leu148del | |
XM_011509417.1:c.430_444del | XP_011507719.1:p.Glu144_Leu148del | |
XM_011509417.2:c.430_444del | XP_011507719.1:p.Glu144_Leu148del | |
XR_002956281.1:n.1345_1359del | ||
NM_005267.5:c.430_444del MANE Select | NP_005258.2:p.Glu144_Leu148del |