Linked Data
dbSNP Id:
rs1431828407
MyVariant Identifiers:
chr15:g.91565599_91565600insTGG (hg19)
chr15:g.91022369_91022370insTGG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.91022369_91022370insTGG , CM000677.2:g.91022369_91022370insTGG | GRCh38 |
| NC_000015.9:g.91565599_91565600insTGG , CM000677.1:g.91565599_91565600insTGG | GRCh37 |
| NC_000015.8:g.89366603_89366604insTGG | NCBI36 |
| NG_012162.1:g.5234_5235insCCA , LRG_884:g.5234_5235insCCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333371.8:c.-121_-120insCCA MANE Select | ENSP00000327650.4:n.-121_-120insCCA | |
| ENST00000643536.1:c.-121_-120insCCA | ENSP00000494429.1:n.-121_-120insCCA | |
| ENST00000333371.7:c.-121_-120insCCA | ENSP00000327650.3:n.-121_-120insCCA | |
| ENST00000535906.1:c.-121_-120insCCA | ENSP00000444053.1:n.-121_-120insCCA | |
| ENST00000556096.6:n.234_235insCCA | ||
| ENST00000557358.1:n.227_228insCCA | ||
| ENST00000574755.5:c.-121_-120insCCA | ENSP00000460413.1:n.-121_-120insCCA | |
| NM_001289148.1:c.-121_-120insCCA | NP_001276077.1:n.-121_-120insCCA | |
| NM_001289149.1:c.-332_-331insCCA | NP_001276078.1:n.-332_-331insCCA | |
| NM_018668.4:c.-121_-120insCCA , LRG_884t1:c.-121_-120insCCA | NP_061138.3:n.-121_-120insCCA | |
| XM_005254884.2:c.-121_-120insCCA | XP_005254941.1:n.-121_-120insCCA | |
| XM_005254887.1:c.-251_-250insCCA | XP_005254944.1:n.-251_-250insCCA | |
| XM_005254888.2:c.-121_-120insCCA | XP_005254945.1:n.-121_-120insCCA | |
| XM_011521448.1:c.-434_-433insCCA | XP_011519750.1:n.-434_-433insCCA | |
| XM_017022075.2:c.-482_-481insCCA | XP_016877564.1:n.-482_-481insCCA | |
| XM_017022076.1:c.-339_-338insCCA | XP_016877565.1:n.-339_-338insCCA | |
| XR_001751213.2:n.216_217insCCA | ||
| NM_018668.5:c.-121_-120insCCA MANE Select | NP_061138.3:n.-121_-120insCCA |