HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31663788_31663789delinsAG , CM000683.2:g.31663788_31663789delinsAG | GRCh38 |
NC_000021.8:g.33036101_33036102delinsAG , CM000683.1:g.33036101_33036102delinsAG | GRCh37 |
NC_000021.7:g.31957972_31957973delinsAG | NCBI36 |
NG_008689.1:g.9167_9168delinsAG , LRG_652:g.9167_9168delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.73-2_73-1delinsAG MANE Select | ENSP00000270142.7:n.73-2_73-1delinsAG | |
ENST00000270142.10:c.73-2_73-1delinsAG | ENSP00000270142.6:n.73-2_73-1delinsAG | |
ENST00000389995.4:c.16-2_16-1delinsAG | ENSP00000374645.4:n.16-2_16-1delinsAG | |
ENST00000470944.1:n.1001-2_1001-1delinsAG | ||
ENST00000476106.5:n.336-2_336-1delinsAG | ||
NM_000454.4:c.73-2_73-1delinsAG , LRG_652t1:c.73-2_73-1delinsAG | NP_000445.1:n.73-2_73-1delinsAG | |
NM_000454.5:c.73-2_73-1delinsAG MANE Select | NP_000445.1:n.73-2_73-1delinsAG |