HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20189544_20189545delinsAC , CM000675.2:g.20189544_20189545delinsAC | GRCh38 |
NC_000013.10:g.20763683_20763684delinsAC , CM000675.1:g.20763683_20763684delinsAC | GRCh37 |
NC_000013.9:g.19661683_19661684delinsAC | NCBI36 |
NG_008358.1:g.8431_8432delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.37_38delinsGT | ENSP00000372295.1:p.Val13= | |
ENST00000382848.5:c.37_38delinsGT MANE Select | ENSP00000372299.4:p.Val13= | |
ENST00000382844.1:c.37_38delinsGT | ENSP00000372295.1:p.Val13= | |
ENST00000382848.4:c.37_38delinsGT | ENSP00000372299.4:p.Val13= | |
NM_004004.5:c.37_38delinsGT | NP_003995.2:p.Val13= | |
XM_011535049.1:c.37_38delinsGT | XP_011533351.1:p.Val13= | |
XM_011535049.2:c.37_38delinsGT | XP_011533351.1:p.Val13= | |
NM_004004.6:c.37_38delinsGT MANE Select | NP_003995.2:p.Val13= |