HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571677_154571678insT , CM000663.2:g.154571677_154571678insT | GRCh38 |
NC_000001.10:g.154544153_154544154insT , CM000663.1:g.154544153_154544154insT | GRCh37 |
NC_000001.9:g.152810777_152810778insT | NCBI36 |
NG_008027.1:g.8897_8898insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.854_855insT MANE Select | ENSP00000357461.3:p.Lys285AsnfsTer? | |
ENST00000636034.1:c.854_855insT | ENSP00000489703.1:p.Lys285AsnfsTer? | |
ENST00000637900.1:c.860_861insT | ENSP00000490474.1:p.Lys287AsnfsTer? | |
ENST00000368476.3:c.854_855insT | ENSP00000357461.3:p.Lys285AsnfsTer? | |
NM_000748.2:c.854_855insT | NP_000739.1:p.Lys285AsnfsTer? | |
XM_017000180.2:c.344_345insT | XP_016855669.1:p.Lys115AsnfsTer? | |
XR_001736952.2:n.1106_1107insT | ||
NM_000748.3:c.854_855insT MANE Select | NP_000739.1:p.Lys285AsnfsTer? |