HGVS | Genome Assembly |
---|---|
NC_000015.10:g.90501184_90501185delinsTA , CM000677.2:g.90501184_90501185delinsTA | GRCh38 |
NC_000015.9:g.91044416_91044417delinsTA , CM000677.1:g.91044416_91044417delinsTA | GRCh37 |
NC_000015.8:g.88845420_88845421delinsTA | NCBI36 |
NG_052946.1:g.117944_117945delinsTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000268182.10:c.*1076_*1077delinsTA MANE Select | ENSP00000268182.5:n.*1076_*1077delinsTA | |
ENST00000268182.9:c.*1076_*1077delinsTA | ENSP00000268182.5:n.*1076_*1077delinsTA | |
ENST00000558957.1:n.2108_2109delinsTA | ||
ENST00000561086.1:n.1817_1818delinsTA | ||
NM_003870.3:c.*1076_*1077delinsTA | NP_003861.1:n.*1076_*1077delinsTA | |
XR_001751409.2:n.6179_6180delinsTA | ||
NM_003870.4:c.*1076_*1077delinsTA MANE Select | NP_003861.1:n.*1076_*1077delinsTA |