HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65170006_65170007insTC , CM000674.2:g.65170006_65170007insTC | GRCh38 |
NC_000012.11:g.65563786_65563787insTC , CM000674.1:g.65563786_65563787insTC | GRCh37 |
NC_000012.10:g.63850053_63850054insTC | NCBI36 |
NG_016210.1:g.5436_5437insTC | |
NG_016210.2:g.5436_5437insTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.410_411insTC MANE Select | ENSP00000308369.2:p.Gly138ArgfsTer? | |
ENST00000308330.2:c.410_411insTC | ENSP00000308369.2:p.Gly138ArgfsTer? | |
ENST00000541171.1:n.424_425insTC | ||
NM_001167614.1:c.410_411insTC | NP_001161086.1:p.Gly138ArgfsTer? | |
NM_014319.4:c.410_411insTC | NP_055134.2:p.Gly138ArgfsTer? | |
NM_014319.5:c.410_411insTC MANE Select | NP_055134.2:p.Gly138ArgfsTer? | |
NM_001167614.2:c.410_411insTC | NP_001161086.1:p.Gly138ArgfsTer? |