HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31667631_31667632del , CM000683.2:g.31667631_31667632del | GRCh38 |
NC_000021.8:g.33039944_33039945del , CM000683.1:g.33039944_33039945del | GRCh37 |
NC_000021.7:g.31961815_31961816del | NCBI36 |
NG_008689.1:g.13010_13011del , LRG_652:g.13010_13011del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.357+256_357+257del MANE Select | ENSP00000270142.7:n.357+256_357+257del | |
ENST00000270142.10:c.357+256_357+257del | ENSP00000270142.6:n.357+256_357+257del | |
ENST00000389995.4:c.300+256_300+257del | ENSP00000374645.4:n.300+256_300+257del | |
ENST00000470944.1:n.1285+256_1285+257del | ||
NM_000454.4:c.357+256_357+257del , LRG_652t1:c.357+256_357+257del | NP_000445.1:n.357+256_357+257del | |
NM_000454.5:c.357+256_357+257del MANE Select | NP_000445.1:n.357+256_357+257del |