HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47003865_47003866delinsAG , CM000681.2:g.47003865_47003866delinsAG | GRCh38 |
NC_000019.9:g.47507122_47507123delinsAG , CM000681.1:g.47507122_47507123delinsAG | GRCh37 |
NC_000019.8:g.52198962_52198963delinsAG | NCBI36 |
NG_047014.1:g.90299_90300delinsAG | |
NG_047014.2:g.147869_147870delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7677_7678delinsAG | ENSP00000385720.2:n.7677_7678delinsAG | |
ENST00000672722.1:c.*3177_*3178delinsAG MANE Select | ENSP00000500409.1:n.*3177_*3178delinsAG | |
ENST00000404338.7:c.7677_7678delinsAG | ENSP00000385720.2:n.7677_7678delinsAG | |
ENST00000614079.1:c.7254_7255delinsAG | ENSP00000483730.1:n.7254_7255delinsAG | |
NM_004491.4:c.7677_7678delinsAG | NP_004482.4:n.7677_7678delinsAG | |
NM_004491.5:c.*3177_*3178delinsAG MANE Select | NP_004482.4:n.*3177_*3178delinsAG |