HGVS | Genome Assembly |
---|---|
NC_000022.11:g.19724398_19724399insA , CM000684.2:g.19724398_19724399insA | GRCh38 |
NC_000022.10:g.19711921_19711922insA , CM000684.1:g.19711921_19711922insA | GRCh37 |
NC_000022.9:g.18091921_18091922insA | NCBI36 |
NG_007974.1:g.5856_5857insA , LRG_478:g.5856_5857insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366425.4:c.555_556insA (GP1BB) MANE Select | ENSP00000383382.2:p.Ala186SerfsTer? | |
ENST00000366425.3:c.555_556insA (GP1BB) | ENSP00000383382.2:p.Ala186SerfsTer? | |
ENST00000431044.5:c.*1640_*1641insA (SEPTIN5) | ENSP00000399685.1:n.*1640_*1641insA | |
NM_000407.4:c.555_556insA , LRG_478t1:c.555_556insA (GP1BB) | NP_000398.1:p.Ala186SerfsTer? | |
NR_037611.1:n.4295_4296insA | ||
NR_037612.1:n.2799_2800insA | ||
NM_000407.5:c.555_556insA (GP1BB) MANE Select | NP_000398.1:p.Ala186SerfsTer? |