HGVS | Genome Assembly |
---|---|
NC_000003.12:g.71772822dup , CM000665.2:g.71772822dup | GRCh38 |
NC_000003.11:g.71821973dup , CM000665.1:g.71821973dup | GRCh37 |
NC_000003.10:g.71904663dup | NCBI36 |
NG_008275.1:g.17390dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295619.4:c.297dup MANE Select | ENSP00000295619.3:p.Gly100TrpfsTer22 | |
ENST00000295619.3:c.297dup | ENSP00000295619.3:p.Gly100TrpfsTer22 | |
ENST00000353065.7:c.234dup | ENSP00000295618.3:p.Gly79TrpfsTer22 | |
NM_001126128.1:c.297dup | NP_001119600.1:p.Gly100TrpfsTer22 | |
NM_021935.3:c.234dup | NP_068754.1:p.Gly79TrpfsTer22 | |
XM_017006974.1:c.237dup | XP_016862463.1:p.Gly80TrpfsTer22 | |
NM_001126128.2:c.297dup MANE Select | NP_001119600.1:p.Gly100TrpfsTer22 | |
NM_021935.4:c.234dup | NP_068754.1:p.Gly79TrpfsTer22 |