HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110573545dup , CM000672.2:g.110573545dup | GRCh38 |
NC_000010.10:g.112333303dup , CM000672.1:g.112333303dup | GRCh37 |
NC_000010.9:g.112323293dup | NCBI36 |
NG_012217.1:g.10855dup , LRG_774:g.10855dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.225-162dup | ||
ENST00000687823.1:n.45-1791dup | ||
ENST00000689932.1:n.403dup | ||
ENST00000691297.1:n.225-162dup | ||
ENST00000691527.1:n.182-162dup | ||
ENST00000692792.1:n.211-162dup | ||
ENST00000361804.5:c.92-162dup MANE Select | ENSP00000354720.5:n.92-162dup | |
ENST00000361804.4:c.92-162dup | ENSP00000354720.4:n.92-162dup | |
ENST00000462899.1:n.238-162dup | ||
NM_005445.3:c.92-162dup , LRG_774t1:c.92-162dup | NP_005436.1:n.92-162dup | |
NM_005445.4:c.92-162dup MANE Select | NP_005436.1:n.92-162dup |