HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21748580_21748583delinsATCCG , CM000669.2:g.21748580_21748583delinsATCCG | GRCh38 |
NC_000007.13:g.21788198_21788201delinsATCCG , CM000669.1:g.21788198_21788201delinsATCCG | GRCh37 |
NC_000007.12:g.21754723_21754726delinsATCCG | NCBI36 |
NG_012886.2:g.210366_210369delinsATCCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.8511_8514delinsATCCG MANE Select | ENSP00000475939.1:p.Cys2838SerfsTer? | |
ENST00000328843.10:c.8532_8535delinsATCCG | ENSP00000330671.7:p.Cys2845SerfsTer? | |
ENST00000409508.7:c.8511_8514delinsATCCG | ENSP00000475939.1:p.Cys2838SerfsTer? | |
ENST00000620169.4:c.8532_8535delinsATCCG | ENSP00000481693.1:p.Cys2845SerfsTer? | |
NM_001277115.1:c.8511_8514delinsATCCG | NP_001264044.1:p.Cys2838SerfsTer? | |
NM_001277115.2:c.8511_8514delinsATCCG MANE Select | NP_001264044.1:p.Cys2838SerfsTer? |