HGVS | Genome Assembly |
---|---|
NC_000002.12:g.27084848_27084849delinsTA , CM000664.2:g.27084848_27084849delinsTA | GRCh38 |
NC_000002.11:g.27307716_27307717delinsTA , CM000664.1:g.27307716_27307717delinsTA | GRCh37 |
NC_000002.10:g.27161220_27161221delinsTA | NCBI36 |
NG_012199.1:g.3106_3107delinsTA | |
NG_046849.1:g.11282_11283delinsTA | |
NG_012199.2:g.3106_3107delinsTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000380320.9:c.2558-143_2558-142delinsTA MANE Select | ENSP00000369677.4:n.2558-143_2558-142deli... | |
ENST00000380320.8:c.2558-143_2558-142delinsTA | ENSP00000369677.4:n.2558-143_2558-142deli... | |
ENST00000433140.1:c.550-143_550-142delinsTA | ||
NM_007046.3:c.2558-143_2558-142delinsTA | NP_008977.1:n.2558-143_2558-142delinsTA | |
XM_006711928.2:c.2558-143_2558-142delinsTA | XP_006711991.1:n.2558-143_2558-142delinsT... | |
NM_007046.4:c.2558-143_2558-142delinsTA MANE Select | NP_008977.1:n.2558-143_2558-142delinsTA |