Linked Data
dbSNP Id:
rs1565872272
gnomAD v2:
11-119149043-A-AATT
gnomAD v4:
11-119278333-A-AATT
MyVariant Identifiers:
chr11:g.119149043_119149044insATT (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119278335_119278336insTAT , CM000673.2:g.119278335_119278336insTAT | GRCh38 |
| NC_000011.9:g.119149045_119149046insTAT , CM000673.1:g.119149045_119149046insTAT | GRCh37 |
| NC_000011.8:g.118654255_118654256insTAT | NCBI36 |
| NG_016808.1:g.77056_77057insTAT , LRG_608:g.77056_77057insTAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700472.1:c.*679+38_*679+39insTAT | ENSP00000515005.1:n.*679+38_*679+39insTAT | |
| ENST00000264033.6:c.1227+38_1227+39insTAT MANE Select | ENSP00000264033.3:n.1227+38_1227+39insTAT | |
| ENST00000637974.1:c.1221+38_1221+39insTAT | ENSP00000490763.1:n.1221+38_1221+39insTAT | |
| ENST00000264033.5:c.1227+38_1227+39insTAT | ENSP00000264033.3:n.1227+38_1227+39insTAT | |
| ENST00000634586.1:c.1227+38_1227+39insTAT | ENSP00000489218.1:n.1227+38_1227+39insTAT | |
| ENST00000634840.1:c.1227+38_1227+39insTAT | ENSP00000489324.1:n.1227+38_1227+39insTAT | |
| NM_005188.3:c.1227+38_1227+39insTAT , LRG_608t1:c.1227+38_1227+39insTAT | NP_005179.2:n.1227+38_1227+39insTAT | |
| XM_011543057.1:c.1227+38_1227+39insTAT | XP_011541359.1:n.1227+38_1227+39insTAT | |
| NM_005188.4:c.1227+38_1227+39insTAT MANE Select | NP_005179.2:n.1227+38_1227+39insTAT |