HGVS | Genome Assembly |
---|---|
NC_000008.11:g.37965919_37965920insT , CM000670.2:g.37965919_37965920insT | GRCh38 |
NC_000008.10:g.37823437_37823438insT , CM000670.1:g.37823437_37823438insT | GRCh37 |
NC_000008.9:g.37942594_37942595insT | NCBI36 |
NG_011936.1:g.5747_5748insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000345060.5:c.550_551insA MANE Select | ENSP00000343782.3:p.Ala184AspfsTer? | |
ENST00000520341.2:n.678_679insA | ||
ENST00000647937.1:c.34_35insA | ENSP00000497740.1:p.Ala12AspfsTer? | |
ENST00000345060.4:c.550_551insA | ENSP00000343782.3:p.Ala184AspfsTer? | |
ENST00000614635.1:c.550_551insA | ENSP00000480325.1:p.Ala184AspfsTer? | |
NM_000025.2:c.550_551insA | NP_000016.1:p.Ala184AspfsTer? | |
NM_000025.3:c.550_551insA MANE Select | NP_000016.1:p.Ala184AspfsTer? |