Linked Data
dbSNP Id:
rs1369960347
MyVariant Identifiers:
chr3:g.143426230_143426231insCG (hg19)
chr3:g.143707388_143707389insCG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.143707389_143707390insGC , CM000665.2:g.143707389_143707390insGC | GRCh38 |
| NC_000003.11:g.143426231_143426232insGC , CM000665.1:g.143426231_143426232insGC | GRCh37 |
| NC_000003.10:g.144908921_144908922insGC | NCBI36 |
| NG_017077.1:g.146143_146144insCG | |
| NG_017077.2:g.146143_146144insCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316549.11:c.534-14082_534-14081insCG MANE Select | ENSP00000320246.6:n.534-14082_534-14081insCG | |
| ENST00000316549.10:c.534-14082_534-14081insCG | ENSP00000320246.6:n.534-14082_534-14081insCG | |
| ENST00000474727.2:c.*145-14082_*145-14081insCG | ENSP00000419090.2:n.*145-14082_*145-14081insCG | |
| NM_173653.3:c.534-14082_534-14081insCG | NP_775924.1:n.534-14082_534-14081insCG | |
| XM_011512704.1:c.534-14082_534-14081insCG | XP_011511006.1:n.534-14082_534-14081insCG | |
| XM_011512704.3:c.534-14082_534-14081insCG | XP_011511006.1:n.534-14082_534-14081insCG | |
| XM_017006202.2:c.534-14082_534-14081insCG | XP_016861691.1:n.534-14082_534-14081insCG | |
| XM_017006203.1:c.183-14082_183-14081insCG | XP_016861692.1:n.183-14082_183-14081insCG | |
| NM_173653.4:c.534-14082_534-14081insCG MANE Select | NP_775924.1:n.534-14082_534-14081insCG |