HGVS | Genome Assembly |
---|---|
NC_000020.11:g.1994218_1994219insGCA , CM000682.2:g.1994218_1994219insGCA | GRCh38 |
NC_000020.10:g.1974864_1974865insGCA , CM000682.1:g.1974864_1974865insGCA | GRCh37 |
NC_000020.9:g.1922864_1922865insGCA | NCBI36 |
NG_028027.1:g.5029_5030insCTG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651882.1:c.-383_-382insCTG (PDYN) | ENSP00000498752.1:n.-383_-382insCTG | |
ENST00000539905.5:c.-326_-325insCTG (PDYN) | ENSP00000440185.1:n.-326_-325insCTG | |
NM_001190898.2:c.-383_-382insCTG (PDYN) | NP_001177827.1:n.-383_-382insCTG | |
NM_001190899.2:c.-326_-325insCTG (PDYN) | NP_001177828.1:n.-326_-325insCTG | |
NM_024411.4:c.-386_-385insCTG (PDYN) | NP_077722.1:n.-386_-385insCTG | |
XR_244229.1:n.1217-12714_1217-12713insGCA (PDYN-AS1) | ||
NR_134520.1:n.1253-12714_1253-12713insGCA (PDYN-AS1) |