HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135859001_135859006delinsCCACCT , CM000664.2:g.135859001_135859006delinsCCACCT | GRCh38 |
NC_000002.11:g.136616571_136616576delinsCCACCT , CM000664.1:g.136616571_136616576delinsCCACCT | GRCh37 |
NC_000002.10:g.136333041_136333046delinsCCACCT | NCBI36 |
NG_008104.2:g.1164_1169delinsAGGTGG , LRG_338:g.1164_1169delinsAGGTGG | |
NG_008958.1:g.22436_22441delinsAGGTGG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264156.3:c.1362+295_1362+300delinsAGGTGG MANE Select | ENSP00000264156.2:n.1362+295_1362+300deli... | |
ENST00000264156.2:c.1362+295_1362+300delinsAGGTGG | ENSP00000264156.2:n.1362+295_1362+300deli... | |
ENST00000492091.1:n.181+3601_181+3606delinsAGGTGG | ||
NM_005915.5:c.1362+295_1362+300delinsAGGTGG | NP_005906.2:n.1362+295_1362+300delinsAGGT... | |
NM_005915.6:c.1362+295_1362+300delinsAGGTGG MANE Select | NP_005906.2:n.1362+295_1362+300delinsAGGT... |