HGVS | Genome Assembly |
---|---|
NC_000011.10:g.119341451del , CM000673.2:g.119341451del | GRCh38 |
NC_000011.9:g.119212161del , CM000673.1:g.119212161del | GRCh37 |
NC_000011.8:g.118717371del | NCBI36 |
NG_012235.1:g.10223del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619721.6:c.*97del (MFRP) MANE Select | ENSP00000481824.1:n.*97del | |
ENST00000360167.4:c.*97del (MFRP) | ENSP00000353291.4:n.*97del | |
ENST00000619721.5:c.*97del (MFRP) | ENSP00000481824.1:n.*97del | |
NM_015645.4:c.-800del (C1QTNF5) | NP_056460.1:n.-800del | |
NM_031433.3:c.*97del (MFRP) | NP_113621.1:n.*97del | |
NM_031433.4:c.*97del (MFRP) MANE Select | NP_113621.1:n.*97del | |
NM_015645.5:c.-800del (C1QTNF5) | NP_056460.1:n.-800del |