HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44388291_44388292delinsAT , CM000667.2:g.44388291_44388292delinsAT | GRCh38 |
NC_000005.9:g.44388393_44388394delinsAT , CM000667.1:g.44388393_44388394delinsAT | GRCh37 |
NC_000005.8:g.44424150_44424151delinsAT | NCBI36 |
NG_011446.1:g.5391_5392delinsAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264664.5:c.325+66_325+67delinsAT MANE Select | ENSP00000264664.4:n.325+66_325+67delinsAT | |
ENST00000264664.4:c.325+66_325+67delinsAT | ENSP00000264664.4:n.325+66_325+67delinsAT | |
NM_004465.1:c.325+66_325+67delinsAT | NP_004456.1:n.325+66_325+67delinsAT | |
XM_005248264.2:c.325+66_325+67delinsAT | XP_005248321.1:n.325+66_325+67delinsAT | |
XM_005248264.4:c.325+66_325+67delinsAT | XP_005248321.1:n.325+66_325+67delinsAT | |
NM_004465.2:c.325+66_325+67delinsAT MANE Select | NP_004456.1:n.325+66_325+67delinsAT |