HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119672528_119672533del , CM000672.2:g.119672528_119672533del | GRCh38 |
NC_000010.10:g.121432040_121432045del , CM000672.1:g.121432040_121432045del | GRCh37 |
NC_000010.9:g.121422030_121422035del | NCBI36 |
NG_016125.1:g.26159_26164del , LRG_742:g.26159_26164del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369085.8:c.781_786del MANE Select | ENSP00000358081.4:p.Arg261_Ala262del | |
ENST00000369085.7:c.781_786del | ENSP00000358081.3:p.Arg261_Ala262del | |
ENST00000450186.1:c.607_612del | ENSP00000410036.1:p.Arg203_Ala204del | |
NM_004281.3:c.781_786del , LRG_742t1:c.781_786del | NP_004272.2:p.Arg261_Ala262del | |
XM_005270287.1:c.781_786del | XP_005270344.1:p.Arg261_Ala262del | |
XM_005270287.2:c.781_786del | XP_005270344.1:p.Arg261_Ala262del | |
NM_004281.4:c.781_786del MANE Select | NP_004272.2:p.Arg261_Ala262del |