Linked Data
gnomAD v4:
12-107001375-G-GA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.107001378dup , CM000674.2:g.107001378dup | GRCh38 |
| NC_000012.11:g.107395156dup , CM000674.1:g.107395156dup | GRCh37 |
| NC_000012.10:g.105919286dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000008527.10:c.596-8dup MANE Select | ENSP00000008527.5:n.596-8dup | |
| ENST00000008527.9:c.596-8dup | ENSP00000008527.5:n.596-8dup | |
| ENST00000546722.1:n.89-8dup | ||
| ENST00000552790.5:n.1155-8dup | ||
| NM_004075.4:c.596-8dup | NP_004066.1:n.596-8dup | |
| XM_011537939.1:c.512-8dup | XP_011536241.1:n.512-8dup | |
| XM_017018832.2:c.512-8dup | XP_016874321.1:n.512-8dup | |
| XM_024448844.1:c.596-8dup | XP_024304612.1:n.596-8dup | |
| XM_024448845.1:c.512-8dup | XP_024304613.1:n.512-8dup | |
| NM_004075.5:c.596-8dup MANE Select | NP_004066.1:n.596-8dup |