HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135031861del , CM000667.2:g.135031861del | GRCh38 |
NC_000005.9:g.134367551del , CM000667.1:g.134367551del | GRCh37 |
NC_000005.8:g.134395450del | NCBI36 |
NG_012114.1:g.7418del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000265340.12:c.170-349del MANE Select | ENSP00000265340.6:n.170-349del | |
ENST00000265340.11:c.170-349del | ENSP00000265340.6:n.170-349del | |
ENST00000502676.1:c.170-349del | ENSP00000423624.1:n.170-349del | |
ENST00000503586.1:c.292-349del | ||
ENST00000504936.1:n.154del | ||
ENST00000506438.5:c.170-349del | ENSP00000427542.1:n.170-349del | |
ENST00000507253.5:c.170-349del | ENSP00000422908.1:n.170-349del | |
NM_002653.4:c.170-349del | NP_002644.4:n.170-349del | |
NM_002653.5:c.170-349del MANE Select | NP_002644.4:n.170-349del |