Linked Data
ClinVar Variation Id:
452189
dbSNP Id:
rs1170759657
gnomAD v2:
3-49142109-CCTT-C
gnomAD v3:
3-49104676-CCTT-C
gnomAD v4:
3-49104676-CCTT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49104679_49104681del , CM000665.2:g.49104679_49104681del | GRCh38 |
| NC_000003.11:g.49142112_49142114del , CM000665.1:g.49142112_49142114del | GRCh37 |
| NC_000003.10:g.49117116_49117118del | NCBI36 |
| NG_042312.1:g.5451_5453del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306125.12:c.55_57del MANE Select | ENSP00000307567.6:p.Lys19del | |
| ENST00000306125.11:c.55_57del | ENSP00000307567.6:p.Lys19del | |
| ENST00000414533.5:c.55_57del | ENSP00000390015.1:p.Lys19del | |
| ENST00000417025.2:n.81_83del | ||
| ENST00000418549.3:c.55_57del | ENSP00000415247.1:p.Lys19del | |
| ENST00000430182.5:c.55_57del | ENSP00000389823.1:p.Lys19del | |
| ENST00000452739.5:c.55_57del | ENSP00000392850.2:p.Lys19del | |
| ENST00000470619.6:n.74_76del | ||
| ENST00000479495.5:n.98-208_98-206del | ||
| ENST00000482261.7:n.131_133del | ||
| ENST00000482438.2:n.81_83del | ||
| ENST00000494767.2:c.55_57del | ENSP00000489170.1:p.Lys19del | |
| ENST00000634359.1:n.198-208_198-206del | ||
| ENST00000634527.1:c.-318-208_-318-206del | ENSP00000489039.1:n.-318-208_-318-206del | |
| ENST00000634602.1:c.55_57del | ENSP00000489082.1:p.Lys19del | |
| ENST00000634609.1:n.80_82del | ||
| ENST00000634724.1:n.79_81del | ||
| ENST00000634802.1:c.55_57del | ENSP00000488917.1:p.Lys19del | |
| ENST00000634953.1:n.82_84del | ||
| ENST00000635052.1:c.55_57del | ENSP00000489409.1:p.Lys19del | |
| ENST00000635194.1:c.55_57del | ENSP00000488960.1:p.Lys19del | |
| ENST00000635231.1:c.55_57del | ENSP00000489550.1:p.Lys19del | |
| ENST00000635278.1:n.79_81del | ||
| ENST00000635443.1:c.55_57del | ENSP00000489154.1:p.Lys19del | |
| ENST00000635494.1:c.55_57del | ENSP00000489331.1:p.Lys19del | |
| ENST00000635501.1:n.445_447del | ||
| ENST00000635622.1:c.-409_-407del | ENSP00000489558.1:n.-409_-407del | |
| NM_001272073.1:c.55_57del | NP_001259002.1:p.Lys19del | |
| NM_005051.2:c.55_57del | NP_005042.1:p.Lys19del | |
| NR_073590.1:n.451_453del | ||
| XM_011533973.1:c.109_111del | XP_011532275.1:p.Lys37del | |
| XM_017006965.2:c.55_57del | XP_016862454.2:p.Lys19del | |
| NM_005051.3:c.55_57del MANE Select | NP_005042.1:p.Lys19del | |
| NM_001272073.2:c.55_57del | NP_001259002.1:p.Lys19del | |
| NR_073590.2:n.79_81del |