Linked Data
dbSNP Id:
rs138856021
gnomAD v4:
10-110573575-C-CCGT
MyVariant Identifiers:
chr10:g.112333333_112333334insCGT (hg19)
chr10:g.110573575_110573576insCGT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110573575_110573576insCGT , CM000672.2:g.110573575_110573576insCGT | GRCh38 |
| NC_000010.10:g.112333333_112333334insCGT , CM000672.1:g.112333333_112333334insCGT | GRCh37 |
| NC_000010.9:g.112323323_112323324insCGT | NCBI36 |
| NG_012217.1:g.10885_10886insCGT , LRG_774:g.10885_10886insCGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.225-132_225-131insCGT | ||
| ENST00000687823.1:n.45-1761_45-1760insCGT | ||
| ENST00000689932.1:n.433_434insCGT | ||
| ENST00000691297.1:n.225-132_225-131insCGT | ||
| ENST00000691527.1:n.182-132_182-131insCGT | ||
| ENST00000692792.1:n.211-132_211-131insCGT | ||
| ENST00000361804.5:c.92-132_92-131insCGT MANE Select | ENSP00000354720.5:n.92-132_92-131insCGT | |
| ENST00000361804.4:c.92-132_92-131insCGT | ENSP00000354720.4:n.92-132_92-131insCGT | |
| ENST00000462899.1:n.238-132_238-131insCGT | ||
| NM_005445.3:c.92-132_92-131insCGT , LRG_774t1:c.92-132_92-131insCGT | NP_005436.1:n.92-132_92-131insCGT | |
| NM_005445.4:c.92-132_92-131insCGT MANE Select | NP_005436.1:n.92-132_92-131insCGT |