Linked Data
dbSNP Id:
rs1178583151
gnomAD v2:
11-61161274-G-GTCC
gnomAD v3:
11-61393802-G-GTCC
gnomAD v4:
11-61393802-G-GTCC
MyVariant Identifiers:
chr11:g.61161274_61161275insTCC (hg19)
chr11:g.61393802_61393803insTCC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61393805_61393807dup , CM000673.2:g.61393805_61393807dup | GRCh38 |
| NC_000011.9:g.61161277_61161279dup , CM000673.1:g.61161277_61161279dup | GRCh37 |
| NC_000011.8:g.60917853_60917855dup | NCBI36 |
| NG_032976.1:g.6446_6448dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334888.10:c.137-79_137-77dup | ENSP00000334844.5:n.137-79_137-77dup | |
| ENST00000544795.6:n.414-79_414-77dup | ||
| ENST00000684926.1:n.153-79_153-77dup | ||
| ENST00000688959.1:c.-123-79_-123-77dup | ENSP00000509213.1:n.-123-79_-123-77dup | |
| ENST00000690736.1:c.137-79_137-77dup | ENSP00000508542.1:n.137-79_137-77dup | |
| ENST00000515837.7:c.137-79_137-77dup MANE Select | ENSP00000440638.1:n.137-79_137-77dup | |
| ENST00000334888.9:c.137-79_137-77dup | ENSP00000334844.5:n.137-79_137-77dup | |
| ENST00000398979.7:c.-47-79_-47-77dup | ENSP00000381950.3:n.-47-79_-47-77dup | |
| ENST00000515837.6:c.137-79_137-77dup | ENSP00000440638.1:n.137-79_137-77dup | |
| ENST00000541473.1:n.151-79_151-77dup | ||
| ENST00000544795.5:n.153-79_153-77dup | ||
| NM_001173990.2:c.137-79_137-77dup | NP_001167461.1:n.137-79_137-77dup | |
| NM_001173991.2:c.137-79_137-77dup | NP_001167462.1:n.137-79_137-77dup | |
| NM_016499.5:c.-47-79_-47-77dup | NP_057583.2:n.-47-79_-47-77dup | |
| XM_005274039.3:c.-47-79_-47-77dup | XP_005274096.1:n.-47-79_-47-77dup | |
| NM_001330285.1:c.-47-79_-47-77dup | NP_001317214.1:n.-47-79_-47-77dup | |
| XM_005274039.4:c.-47-79_-47-77dup | XP_005274096.1:n.-47-79_-47-77dup | |
| NM_001173990.3:c.137-79_137-77dup MANE Select | NP_001167461.1:n.137-79_137-77dup | |
| NM_001173991.3:c.137-79_137-77dup | NP_001167462.1:n.137-79_137-77dup | |
| NM_001330285.2:c.-47-79_-47-77dup | NP_001317214.1:n.-47-79_-47-77dup | |
| NM_016499.6:c.-47-79_-47-77dup | NP_057583.2:n.-47-79_-47-77dup |