HGVS | Genome Assembly |
---|---|
NC_000002.12:g.165761940dup , CM000664.2:g.165761940dup | GRCh38 |
NC_000002.11:g.166618450dup , CM000664.1:g.166618450dup | GRCh37 |
NC_000002.10:g.166326696dup | NCBI36 |
NG_012069.1:g.37354dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000392701.8:c.803dup MANE Select | ENSP00000376465.3:p.Thr269AsnfsTer3 | |
ENST00000392701.7:c.803dup | ENSP00000376465.3:p.Thr269AsnfsTer3 | |
ENST00000412248.5:c.803dup | ENSP00000412643.1:p.Thr269AsnfsTer3 | |
ENST00000437849.1:c.191dup | ENSP00000391104.1:p.Thr65AsnfsTer3 | |
ENST00000463254.1:n.86dup | ||
NM_004482.3:c.803dup | NP_004473.2:p.Thr269AsnfsTer3 | |
XM_005246449.1:c.803dup | XP_005246506.1:p.Thr269AsnfsTer3 | |
XM_006712402.2:c.803dup | XP_006712465.1:p.Thr269AsnfsTer3 | |
XM_011510929.1:c.803dup | XP_011509231.1:p.Thr269AsnfsTer3 | |
XM_017003770.1:c.803dup | XP_016859259.1:p.Thr269AsnfsTer3 | |
XR_002959253.1:n.1144dup | ||
NM_004482.4:c.803dup MANE Select | NP_004473.2:p.Thr269AsnfsTer3 |