HGVS | Genome Assembly |
---|---|
NC_000013.11:g.110169807_110169808insGGT , CM000675.2:g.110169807_110169808insGGT | GRCh38 |
NC_000013.10:g.110822154_110822155insGGT , CM000675.1:g.110822154_110822155insGGT | GRCh37 |
NC_000013.9:g.109620155_109620156insGGT | NCBI36 |
NG_011544.2:g.142342_142343insACC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375820.10:c.3743-46_3743-45insACC MANE Select | ENSP00000364979.4:n.3743-46_3743-45insACC | |
ENST00000375820.8:c.3743-46_3743-45insACC | ENSP00000364979.4:n.3743-46_3743-45insACC | |
NM_001845.5:c.3743-46_3743-45insACC | NP_001836.3:n.3743-46_3743-45insACC | |
XM_011521048.1:c.3551-46_3551-45insACC | XP_011519350.1:n.3551-46_3551-45insACC | |
XM_011521048.2:c.3551-46_3551-45insACC | XP_011519350.1:n.3551-46_3551-45insACC | |
NM_001845.6:c.3743-46_3743-45insACC MANE Select | NP_001836.3:n.3743-46_3743-45insACC |