Linked Data
dbSNP Id:
rs1364576754
MyVariant Identifiers:
chr12:g.21715650_21715651insGAT (hg19)
chr12:g.21562716_21562717insGAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21562716_21562717insGAT , CM000674.2:g.21562716_21562717insGAT | GRCh38 |
| NC_000012.11:g.21715650_21715651insGAT , CM000674.1:g.21715650_21715651insGAT | GRCh37 |
| NC_000012.10:g.21606917_21606918insGAT | NCBI36 |
| NG_016167.1:g.47131_47132insATC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261195.3:c.1062+201_1062+202insATC MANE Select | ENSP00000261195.2:n.1062+201_1062+202insATC | |
| ENST00000647960.1:c.*1064+201_*1064+202insATC | ENSP00000497202.1:n.*1064+201_*1064+202insATC | |
| ENST00000648372.1:n.989+201_989+202insATC | ||
| ENST00000261195.2:c.1062+201_1062+202insATC | ENSP00000261195.2:n.1062+201_1062+202insATC | |
| NM_021957.3:c.1062+201_1062+202insATC | NP_068776.2:n.1062+201_1062+202insATC | |
| XM_005253352.1:c.1062+201_1062+202insATC | XP_005253409.1:n.1062+201_1062+202insATC | |
| XM_005253354.2:c.843+201_843+202insATC | XP_005253411.1:n.843+201_843+202insATC | |
| XM_006719062.2:c.1062+201_1062+202insATC | XP_006719125.1:n.1062+201_1062+202insATC | |
| XM_006719063.2:c.831+201_831+202insATC | XP_006719126.1:n.831+201_831+202insATC | |
| NM_021957.4:c.1062+201_1062+202insATC MANE Select | NP_068776.2:n.1062+201_1062+202insATC | |
| XM_006719063.3:c.831+201_831+202insATC | XP_006719126.1:n.831+201_831+202insATC | |
| XM_017019245.2:c.1062+201_1062+202insATC | XP_016874734.1:n.1062+201_1062+202insATC | |
| XM_024448960.1:c.1062+201_1062+202insATC | XP_024304728.1:n.1062+201_1062+202insATC |