Linked Data
dbSNP Id:
rs1363884778
gnomAD v3:
9-101425376-C-CTT
gnomAD v4:
9-101425376-C-CTT
MyVariant Identifiers:
chr9:g.104187658_104187659insTT (hg19)
chr9:g.101425376_101425377insTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101425377_101425378insTT , CM000671.2:g.101425377_101425378insTT | GRCh38 |
| NC_000009.11:g.104187659_104187660insTT , CM000671.1:g.104187659_104187660insTT | GRCh37 |
| NC_000009.10:g.103227480_103227481insTT | NCBI36 |
| NG_012387.1:g.15404_15405insAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647789.2:c.799+76_799+77insAA MANE Select | ENSP00000497767.1:n.799+76_799+77insAA | |
| ENST00000648064.1:c.799+76_799+77insAA | ENSP00000497990.1:n.799+76_799+77insAA | |
| ENST00000648758.1:c.799+76_799+77insAA | ENSP00000497731.1:n.799+76_799+77insAA | |
| ENST00000649902.1:c.799+76_799+77insAA | ENSP00000497216.1:n.799+76_799+77insAA | |
| ENST00000374855.8:c.799+76_799+77insAA | ENSP00000363988.4:n.799+76_799+77insAA | |
| ENST00000616752.1:c.799+76_799+77insAA | ENSP00000481363.1:n.799+76_799+77insAA | |
| NM_000035.3:c.799+76_799+77insAA | NP_000026.2:n.799+76_799+77insAA | |
| NM_000035.4:c.799+76_799+77insAA MANE Select | NP_000026.2:n.799+76_799+77insAA |