Linked Data
dbSNP Id:
rs1243883923
gnomAD v2:
6-31784675-T-TTAAAAA
gnomAD v4:
6-31816898-T-TTAAAAA
MyVariant Identifiers:
chr6:g.31784675_31784676insTAAAAA (hg19)
chr6:g.31816898_31816899insTAAAAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31816898_31816899insTAAAAA , CM000668.2:g.31816898_31816899insTAAAAA | GRCh38 |
| NC_000006.11:g.31784675_31784676insTAAAAA , CM000668.1:g.31784675_31784676insTAAAAA | GRCh37 |
| NC_000006.10:g.31892654_31892655insTAAAAA | NCBI36 |
| NG_011855.1:g.3160_3161insTTTTTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375651.7:c.1142_1143insTAAAAA (HSPA1A) MANE Select | ENSP00000364802.5:p.Met381delinsIleLysLys | |
| ENST00000375651.6:c.1142_1143insTAAAAA (HSPA1A) | ENSP00000364802.5:p.Met381delinsIleLysLys | |
| ENST00000608703.1:c.647_648insTAAAAA (HSPA1A) | ENSP00000477378.1:p.Met216delinsIleLysLys | |
| NM_005345.5:c.1142_1143insTAAAAA (HSPA1A) | NP_005336.3:p.Met381delinsIleLysLys | |
| XM_005249073.2:c.-14+4114_-14+4115insTTTTTA (HSPA1L) | XP_005249130.1:n.-14+4114_-14+4115insTTTTTA | |
| XM_011514566.1:c.-14+4114_-14+4115insTTTTTA (HSPA1L) | XP_011512868.1:n.-14+4114_-14+4115insTTTTTA | |
| NM_005345.6:c.1142_1143insTAAAAA (HSPA1A) MANE Select | NP_005336.3:p.Met381delinsIleLysLys |