Linked Data
gnomAD v4:
12-53973809-GCGTCCC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.53973810_53973815del , CM000674.2:g.53973810_53973815del | GRCh38 |
| NC_000012.11:g.54367594_54367599del , CM000674.1:g.54367594_54367599del | GRCh37 |
| NC_000012.10:g.52653861_52653866del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243082.4:c.569_574del (HOXC11) | ENSP00000243082.4:p.Ala190_Arg192delinsGly | |
| ENST00000546378.1:c.569_574del (HOXC11) MANE Select | ENSP00000446680.1:p.Ala190_Arg192delinsGly | |
| NM_014212.3:c.569_574del (HOXC11) | NP_055027.1:p.Ala190_Arg192delinsGly | |
| NR_047517.1:n.59+1083_59+1088del (HOTAIR) | ||
| NM_014212.4:c.569_574del (HOXC11) MANE Select | NP_055027.1:p.Ala190_Arg192delinsGly |