Linked Data
dbSNP Id:
rs1367545512
gnomAD v2:
7-117180193-A-ATAC
gnomAD v4:
7-117540139-A-ATAC
MyVariant Identifiers:
chr7:g.117180193_117180194insTAC (hg19)
chr7:g.117540139_117540140insTAC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117540141_117540143dup , CM000669.2:g.117540141_117540143dup | GRCh38 |
| NC_000007.13:g.117180195_117180197dup , CM000669.1:g.117180195_117180197dup | GRCh37 |
| NC_000007.12:g.116967431_116967433dup | NCBI36 |
| NG_016465.4:g.79358_79360dup , LRG_663:g.79358_79360dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647720.2:c.911_913dup | ENSP00000497673.2:p.Tyr304_Phe305insTyr | |
| ENST00000647978.2:c.*808_*810dup | ENSP00000497658.1:n.*808_*810dup | |
| ENST00000649781.2:c.911_913dup | ENSP00000497203.1:p.Tyr304_Phe305insTyr | |
| ENST00000685018.2:c.911_913dup | ENSP00000510194.2:p.Tyr304_Phe305insTyr | |
| ENST00000687278.2:c.911_913dup | ENSP00000509593.2:p.Tyr304_Phe305insTyr | |
| ENST00000699585.1:c.911_913dup | ENSP00000514456.1:p.Tyr304_Phe305insTyr | |
| ENST00000699596.1:c.911_913dup | ENSP00000514465.1:p.Tyr304_Phe305insTyr | |
| ENST00000699597.1:c.911_913dup | ENSP00000514466.1:p.Tyr304_Phe305insTyr | |
| ENST00000699598.1:c.911_913dup | ENSP00000514467.1:p.Tyr304_Phe305insTyr | |
| ENST00000699599.1:c.911_913dup | ENSP00000514468.1:p.Tyr304_Phe305insTyr | |
| ENST00000699600.1:c.911_913dup | ENSP00000514469.1:p.Tyr304_Phe305insTyr | |
| ENST00000699601.1:c.911_913dup | ENSP00000514470.1:p.Tyr304_Phe305insTyr | |
| ENST00000699602.1:c.911_913dup | ENSP00000514471.1:p.Tyr304_Phe305insTyr | |
| ENST00000699604.1:c.*735_*737dup | ENSP00000514472.1:n.*735_*737dup | |
| ENST00000699605.1:c.668_670dup | ENSP00000514473.1:p.Tyr223_Phe224insTyr | |
| ENST00000003084.11:c.911_913dup MANE Select | ENSP00000003084.6:p.Tyr304_Phe305insTyr | |
| ENST00000647978.1:c.*808_*810dup | ENSP00000497658.1:n.*808_*810dup | |
| ENST00000648260.1:c.911_913dup | ENSP00000497957.1:p.Tyr304_Phe305insTyr | |
| ENST00000649406.1:c.911_913dup | ENSP00000497965.1:p.Tyr304_Phe305insTyr | |
| ENST00000649781.1:c.911_913dup | ENSP00000497203.1:p.Tyr304_Phe305insTyr | |
| ENST00000673785.1:c.668_670dup | ENSP00000501235.1:p.Tyr223_Phe224insTyr | |
| ENST00000003084.10:c.911_913dup | ENSP00000003084.6:p.Tyr304_Phe305insTyr | |
| ENST00000426809.5:c.821_823dup | ENSP00000389119.1:p.Tyr274_Phe275insTyr | |
| NM_000492.3:c.911_913dup , LRG_663t1:c.911_913dup | NP_000483.3:p.Tyr304_Phe305insTyr | |
| XM_011515751.1:c.1001_1003dup | XP_011514053.1:p.Tyr334_Phe335insTyr | |
| XM_011515752.1:c.1001_1003dup | XP_011514054.1:p.Tyr334_Phe335insTyr | |
| XM_011515753.1:c.668_670dup | XP_011514055.1:p.Tyr223_Phe224insTyr | |
| XM_011515754.1:c.668_670dup | XP_011514056.1:p.Tyr223_Phe224insTyr | |
| NM_000492.4:c.911_913dup MANE Select | NP_000483.3:p.Tyr304_Phe305insTyr |