Linked Data
dbSNP Id:
rs568299665
gnomAD v2:
6-33132523-CG-C
gnomAD v3:
6-33164746-CG-C
gnomAD v4:
6-33164746-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33164754del , CM000668.2:g.33164754del | GRCh38 |
| NC_000006.11:g.33132531del , CM000668.1:g.33132531del | GRCh37 |
| NC_000006.10:g.33240509del | NCBI36 |
| NG_011589.1:g.32722del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683572.1:n.669+105del | ||
| ENST00000341947.7:c.4863+105del MANE Select | ENSP00000339915.2:n.4863+105del | |
| ENST00000341947.6:c.4863+105del | ENSP00000339915.2:n.4863+105del | |
| ENST00000361917.5:c.4542+105del | ENSP00000355123.1:n.4542+105del | |
| ENST00000374708.8:c.4605+105del | ENSP00000363840.4:n.4605+105del | |
| ENST00000477772.1:n.653+105del | ||
| NM_080679.2:c.4542+105del | NP_542410.2:n.4542+105del | |
| NM_080680.2:c.4863+105del | NP_542411.2:n.4863+105del | |
| NM_080681.2:c.4605+105del | NP_542412.2:n.4605+105del | |
| XM_011514298.1:c.4017+105del | XP_011512600.1:n.4017+105del | |
| XM_011514299.1:c.4149+105del | XP_011512601.1:n.4149+105del | |
| XM_011514300.1:c.3969+105del | XP_011512602.1:n.3969+105del | |
| XM_011514301.1:c.3906+105del | XP_011512603.1:n.3906+105del | |
| XM_011514302.1:c.3750+105del | XP_011512604.1:n.3750+105del | |
| XM_011514299.2:c.4149+105del | XP_011512601.1:n.4149+105del | |
| XM_011514300.2:c.3969+105del | XP_011512602.1:n.3969+105del | |
| XM_011514302.2:c.3750+105del | XP_011512604.1:n.3750+105del | |
| XM_017010250.1:c.4863+105del | XP_016865739.1:n.4863+105del | |
| XM_017010251.2:c.3681+105del | XP_016865740.1:n.3681+105del | |
| NM_080680.3:c.4863+105del MANE Select | NP_542411.2:n.4863+105del | |
| NM_080681.3:c.4605+105del | NP_542412.2:n.4605+105del | |
| NM_080679.3:c.4542+105del | NP_542410.2:n.4542+105del |