Linked Data
ClinVar Variation Id:
97796
dbSNP Id:
rs104895553
gnomAD v3:
19-54940945-T-TC
gnomAD v4:
19-54940945-T-TC
MyVariant Identifiers:
chr19:g.54940945_54940946insC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.54940947dup , CM000681.2:g.54940947dup | GRCh38 |
| NC_000019.8:g.60144127dup | NCBI36 |
| NG_008056.1:g.11560dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592784.6:c.337dup MANE Select | ENSP00000468706.1:p.Glu113GlyfsTer7 | |
| ENST00000328092.9:c.337dup | ENSP00000329568.5:p.Glu113GlyfsTer7 | |
| ENST00000340844.6:c.337dup | ENSP00000339491.2:p.Glu113GlyfsTer7 | |
| ENST00000586379.5:c.337dup | ENSP00000468243.1:p.Glu113GlyfsTer7 | |
| ENST00000588756.5:c.337dup | ENSP00000467123.1:p.Glu113GlyfsTer7 | |
| ENST00000590030.5:c.337dup | ENSP00000465520.1:p.Glu113GlyfsTer7 | |
| ENST00000592784.5:c.337dup | ENSP00000468706.1:p.Glu113GlyfsTer7 | |
| NM_001127255.1:c.337dup | NP_001120727.1:p.Glu113GlyfsTer7 | |
| NM_139176.3:c.337dup | NP_631915.2:p.Glu113GlyfsTer7 | |
| NM_206828.3:c.337dup | NP_996611.2:p.Glu113GlyfsTer7 | |
| XM_006723075.2:c.337dup | XP_006723138.1:p.Glu113GlyfsTer7 | |
| XM_006723076.2:c.337dup | XP_006723139.1:p.Glu113GlyfsTer7 | |
| XM_011526596.1:c.421dup | XP_011524898.1:p.Glu141GlyfsTer7 | |
| XM_011526597.1:c.421dup | XP_011524899.1:p.Glu141GlyfsTer7 | |
| XM_011526598.1:c.421dup | XP_011524900.1:p.Glu141GlyfsTer7 | |
| XM_011526599.1:c.337dup | XP_011524901.1:p.Glu113GlyfsTer7 | |
| XM_011526600.1:c.337dup | XP_011524902.1:p.Glu113GlyfsTer7 | |
| XM_011526601.1:c.421dup | XP_011524903.1:p.Glu141GlyfsTer7 | |
| XR_935761.1:n.855dup | ||
| XM_006723075.3:c.337dup | XP_006723138.1:p.Glu113GlyfsTer7 | |
| XM_006723076.3:c.337dup | XP_006723139.1:p.Glu113GlyfsTer7 | |
| XM_011526596.2:c.421dup | XP_011524898.1:p.Glu141GlyfsTer7 | |
| XM_011526599.2:c.337dup | XP_011524901.1:p.Glu113GlyfsTer7 | |
| XM_011526601.2:c.421dup | XP_011524903.1:p.Glu141GlyfsTer7 |