HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659729dup , CM000683.2:g.31659729dup | GRCh38 |
NC_000021.8:g.33032042dup , CM000683.1:g.33032042dup | GRCh37 |
NC_000021.7:g.31953913dup | NCBI36 |
NG_008689.1:g.5108dup , LRG_652:g.5108dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270142.11:c.-41dup MANE Select | ENSP00000270142.7:n.-41dup | |
ENST00000270142.10:c.-41dup | ENSP00000270142.6:n.-41dup | |
ENST00000389995.4:c.-41dup | ENSP00000374645.4:n.-41dup | |
ENST00000470944.1:n.21dup | ||
ENST00000476106.5:n.37dup | ||
NM_000454.4:c.-41dup , LRG_652t1:c.-41dup | NP_000445.1:n.-41dup | |
NM_000454.5:c.-41dup MANE Select | NP_000445.1:n.-41dup |