HGVS | Genome Assembly |
---|---|
NC_000001.11:g.15445561_15445563dup , CM000663.2:g.15445561_15445563dup | GRCh38 |
NC_000001.10:g.15772056_15772058dup , CM000663.1:g.15772056_15772058dup | GRCh37 |
NC_000001.9:g.15644643_15644645dup | NCBI36 |
NG_009253.1:g.12119_12121dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375949.5:c.640-36_640-34dup MANE Select | ENSP00000365116.4:n.640-36_640-34dup | |
ENST00000375943.6:c.*94-36_*94-34dup | ENSP00000365110.2:n.*94-36_*94-34dup | |
ENST00000375949.4:c.640-36_640-34dup | ENSP00000365116.4:n.640-36_640-34dup | |
ENST00000483406.1:n.404-36_404-34dup | ||
NM_007272.2:c.640-36_640-34dup | NP_009203.2:n.640-36_640-34dup | |
XM_011540550.1:c.494-36_494-34dup | XP_011538852.1:n.494-36_494-34dup | |
NM_007272.3:c.640-36_640-34dup MANE Select | NP_009203.2:n.640-36_640-34dup |