Canonical Allele Identifier:
CA555415609
Gene:
Linked Data
dbSNP Id:
rs1439635305
gnomAD v2:
4-145480635-G-GTTA
gnomAD v3:
4-144559483-G-GTTA
gnomAD v4:
4-144559483-G-GTTA
MyVariant Identifiers:
chr4:g.145480635_145480636insTTA (hg19)
chr4:g.144559483_144559484insTTA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144559484_144559485insTAT , CM000666.2:g.144559484_144559485insTAT | GRCh38 |
| NC_000004.11:g.145480636_145480637insTAT , CM000666.1:g.145480636_145480637insTAT | GRCh37 |
| NC_000004.10:g.145700086_145700087insTAT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-143506_328-143505insTAA | ENSP00000497507.1:n.328-143506_328-143505insTAA | |
| XR_939272.1:n.178+2500_178+2501insTAA | ||
| XR_939273.1:n.178+2500_178+2501insTAA | ||
| XR_939272.2:n.522+2500_522+2501insTAA | ||
| XR_939273.2:n.522+2500_522+2501insTAA |