HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8732074_8732075insA , CM000685.2:g.8732074_8732075insA | GRCh38 |
NC_000023.10:g.8700115_8700116insA , CM000685.1:g.8700115_8700116insA | GRCh37 |
NC_000023.9:g.8660115_8660116insA | NCBI36 |
NG_007088.1:g.5112_5113insT | |
NG_007088.2:g.5112_5113insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262648.8:c.-39_-38insT MANE Select | ENSP00000262648.3:n.-39_-38insT | |
ENST00000262648.7:c.-39_-38insT | ENSP00000262648.3:n.-39_-38insT | |
ENST00000619786.1:c.-39_-38insT | ENSP00000478734.1:n.-39_-38insT | |
NM_000216.2:c.-39_-38insT | NP_000207.2:n.-39_-38insT | |
XM_005274501.3:c.-39_-38insT | XP_005274558.1:n.-39_-38insT | |
NM_000216.3:c.-39_-38insT | NP_000207.2:n.-39_-38insT | |
XM_005274501.4:c.-39_-38insT | XP_005274558.1:n.-39_-38insT | |
NM_000216.4:c.-39_-38insT MANE Select | NP_000207.2:n.-39_-38insT |