HGVS | Genome Assembly |
---|---|
NC_000010.11:g.80275188_80275189insGG , CM000672.2:g.80275188_80275189insGG | GRCh38 |
NC_000010.10:g.82034944_82034945insGG , CM000672.1:g.82034944_82034945insGG | GRCh37 |
NC_000010.9:g.82024924_82024925insGG | NCBI36 |
NG_008083.1:g.19490_19491insCC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000372213.8:c.779_780insCC MANE Select | ENSP00000361287.3:p.Val261LeufsTer? | |
ENST00000372213.7:c.779_780insCC | ENSP00000361287.3:p.Val261LeufsTer? | |
ENST00000480845.1:n.11_12insCC | ||
ENST00000485270.5:n.291_292insCC | ||
NM_000429.2:c.779_780insCC | NP_000420.1:p.Val261LeufsTer? | |
XM_005269842.3:c.779_780insCC | XP_005269899.1:p.Val261LeufsTer? | |
XM_005269843.3:c.656_657insCC | XP_005269900.1:p.Val220LeufsTer? | |
NM_000429.3:c.779_780insCC MANE Select | NP_000420.1:p.Val261LeufsTer? |