HGVS | Genome Assembly |
---|---|
NC_000010.11:g.80275144_80275145insGA , CM000672.2:g.80275144_80275145insGA | GRCh38 |
NC_000010.10:g.82034900_82034901insGA , CM000672.1:g.82034900_82034901insGA | GRCh37 |
NC_000010.9:g.82024880_82024881insGA | NCBI36 |
NG_008083.1:g.19534_19535insTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372213.8:c.823_824insTC MANE Select | ENSP00000361287.3:p.Gly275ValfsTer17 | |
ENST00000372213.7:c.823_824insTC | ENSP00000361287.3:p.Gly275ValfsTer17 | |
ENST00000480845.1:n.55_56insTC | ||
ENST00000485270.5:n.335_336insTC | ||
NM_000429.2:c.823_824insTC | NP_000420.1:p.Gly275ValfsTer17 | |
XM_005269842.3:c.823_824insTC | XP_005269899.1:p.Gly275ValfsTer17 | |
XM_005269843.3:c.700_701insTC | XP_005269900.1:p.Gly234ValfsTer17 | |
NM_000429.3:c.823_824insTC MANE Select | NP_000420.1:p.Gly275ValfsTer17 |