HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942220_94942221delinsGA , CM000672.2:g.94942220_94942221delinsGA | GRCh38 |
NC_000010.10:g.96701977_96701978delinsGA , CM000672.1:g.96701977_96701978delinsGA | GRCh37 |
NC_000010.9:g.96691967_96691968delinsGA | NCBI36 |
NG_008385.1:g.8563_8564delinsGA | |
NG_008385.2:g.9063_9064delinsGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.360_361delinsGA MANE Select | ENSP00000260682.6:p.Trp120= | |
ENST00000643112.1:c.360_361delinsGA | ENSP00000496202.1:p.Trp120= | |
ENST00000645207.1:n.513_514delinsGA | ||
ENST00000260682.6:c.360_361delinsGA | ENSP00000260682.6:p.Trp120= | |
ENST00000461906.1:n.385_386delinsGA | ||
ENST00000473496.1:n.131_132delinsGA | ||
NM_000771.3:c.360_361delinsGA | NP_000762.2:p.Trp120= | |
NM_000771.4:c.360_361delinsGA MANE Select | NP_000762.2:p.Trp120= |