Linked Data
dbSNP Id:
rs754842936
MyVariant Identifiers:
chr12:g.32975610_32975611insTCGGCAAAT (hg19)
chr12:g.32822676_32822677insTCGGCAAAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.32822676_32822677insTCGGCAAAT , CM000674.2:g.32822676_32822677insTCGGCAAAT | GRCh38 |
| NC_000012.11:g.32975610_32975611insTCGGCAAAT , CM000674.1:g.32975610_32975611insTCGGCAAAT | GRCh37 |
| NC_000012.10:g.32866877_32866878insTCGGCAAAT | NCBI36 |
| NG_009000.1:g.79170_79171insATTTGCCGA , LRG_398:g.79170_79171insATTTGCCGA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700555.2:n.187-46_187-45insATTTGCCGA | ||
| ENST00000700559.2:c.1675-46_1675-45insATTTGCCGA | ENSP00000515065.2:n.1675-46_1675-45insATTTGCCGA | |
| ENST00000700563.2:c.1675-46_1675-45insATTTGCCGA | ENSP00000515066.2:n.1675-46_1675-45insATTTGCCGA | |
| ENST00000546498.2:n.362-46_362-45insATTTGCCGA | ||
| ENST00000700555.1:c.115-46_115-45insATTTGCCGA | ENSP00000515062.1:n.115-46_115-45insATTTGCCGA | |
| ENST00000700556.1:c.146-46_146-45insATTTGCCGA | ||
| ENST00000700559.1:c.890-46_890-45insATTTGCCGA | ||
| ENST00000700560.1:n.890-46_890-45insATTTGCCGA | ||
| ENST00000700561.1:n.1016-46_1016-45insATTTGCCGA | ||
| ENST00000700563.1:c.1629-46_1629-45insATTTGCCGA | ||
| ENST00000700564.1:n.1679-46_1679-45insATTTGCCGA | ||
| ENST00000070846.11:c.1807-46_1807-45insATTTGCCGA | ENSP00000070846.6:n.1807-46_1807-45insATTTGCCGA | |
| ENST00000340811.9:c.1675-46_1675-45insATTTGCCGA MANE Select | ENSP00000342800.5:n.1675-46_1675-45insATTTGCCGA | |
| ENST00000070846.10:c.1807-46_1807-45insATTTGCCGA | ENSP00000070846.6:n.1807-46_1807-45insATTTGCCGA | |
| ENST00000340811.8:c.1675-46_1675-45insATTTGCCGA | ENSP00000342800.4:n.1675-46_1675-45insATTTGCCGA | |
| ENST00000546498.1:n.362-46_362-45insATTTGCCGA | ||
| ENST00000552612.5:n.96-46_96-45insATTTGCCGA | ||
| ENST00000613243.1:c.1807-46_1807-45insATTTGCCGA | ENSP00000478295.1:n.1807-46_1807-45insATTTGCCGA | |
| NM_001005242.2:c.1675-46_1675-45insATTTGCCGA | NP_001005242.2:n.1675-46_1675-45insATTTGCCGA | |
| NM_004572.3:c.1807-46_1807-45insATTTGCCGA , LRG_398t1:c.1807-46_1807-45insATTTGCCGA | NP_004563.2:n.1807-46_1807-45insATTTGCCGA | |
| NM_001005242.3:c.1675-46_1675-45insATTTGCCGA MANE Select | NP_001005242.2:n.1675-46_1675-45insATTTGCCGA | |
| NM_004572.4:c.1807-46_1807-45insATTTGCCGA | NP_004563.2:n.1807-46_1807-45insATTTGCCGA |