HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571693_154571700del , CM000663.2:g.154571693_154571700del | GRCh38 |
NC_000001.10:g.154544169_154544176del , CM000663.1:g.154544169_154544176del | GRCh37 |
NC_000001.9:g.152810793_152810800del | NCBI36 |
NG_008027.1:g.8913_8920del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.870_877del MANE Select | ENSP00000357461.3:p.Ser291ArgfsTer? | |
ENST00000636034.1:c.870_877del | ENSP00000489703.1:p.Ser291ArgfsTer? | |
ENST00000637900.1:c.876_883del | ENSP00000490474.1:p.Ser293ArgfsTer? | |
ENST00000368476.3:c.870_877del | ENSP00000357461.3:p.Ser291ArgfsTer? | |
NM_000748.2:c.870_877del | NP_000739.1:p.Ser291ArgfsTer? | |
XM_017000180.2:c.360_367del | XP_016855669.1:p.Ser121ArgfsTer? | |
XR_001736952.2:n.1122_1129del | ||
NM_000748.3:c.870_877del MANE Select | NP_000739.1:p.Ser291ArgfsTer? |