HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8732003_8732004insT , CM000685.2:g.8732003_8732004insT | GRCh38 |
NC_000023.10:g.8700044_8700045insT , CM000685.1:g.8700044_8700045insT | GRCh37 |
NC_000023.9:g.8660044_8660045insT | NCBI36 |
NG_007088.1:g.5183_5184insA | |
NG_007088.2:g.5183_5184insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262648.8:c.33_34insA MANE Select | ENSP00000262648.3:p.Leu12ThrfsTer? | |
ENST00000262648.7:c.33_34insA | ENSP00000262648.3:p.Leu12ThrfsTer? | |
ENST00000619786.1:c.33_34insA | ENSP00000478734.1:p.Leu12ThrfsTer? | |
NM_000216.2:c.33_34insA | NP_000207.2:p.Leu12ThrfsTer? | |
XM_005274501.3:c.33_34insA | XP_005274558.1:p.Leu12ThrfsTer? | |
NM_000216.3:c.33_34insA | NP_000207.2:p.Leu12ThrfsTer? | |
XM_005274501.4:c.33_34insA | XP_005274558.1:p.Leu12ThrfsTer? | |
NM_000216.4:c.33_34insA MANE Select | NP_000207.2:p.Leu12ThrfsTer? |