Linked Data
dbSNP Id:
rs765072353
gnomAD v2:
17-56770197-CCGCCTCAGTCTTCGTTCTCT-C
gnomAD v3:
17-58692836-CCGCCTCAGTCTTCGTTCTCT-C
gnomAD v4:
17-58692836-CCGCCTCAGTCTTCGTTCTCT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58692843_58692862del , CM000679.2:g.58692843_58692862del | GRCh38 |
| NC_000017.10:g.56770204_56770223del , CM000679.1:g.56770204_56770223del | GRCh37 |
| NC_000017.9:g.54125203_54125222del | NCBI36 |
| NG_023199.1:g.5242_5261del , LRG_314:g.5242_5261del | |
| NG_047169.1:g.4224_4243del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.-207+158_-207+177del | ENSP00000464056.2:n.-207+158_-207+177del | |
| ENST00000697675.1:n.271_290del | ||
| ENST00000697676.1:n.205+55_205+74del | ||
| ENST00000697677.1:n.258_277del | ||
| ENST00000697678.1:n.47+211_47+230del | ||
| ENST00000697679.1:n.251_270del | ||
| ENST00000697680.1:c.*41_*60del | ENSP00000513392.1:n.*41_*60del | |
| ENST00000697681.1:c.*41_*60del | ENSP00000513393.1:n.*41_*60del | |
| ENST00000697683.1:c.*41_*60del | ENSP00000513395.1:n.*41_*60del | |
| ENST00000697684.1:n.205+55_205+74del | ||
| ENST00000697685.1:c.*41_*60del | ENSP00000513396.1:n.*41_*60del | |
| ENST00000697686.1:c.-207+211_-207+230del | ENSP00000513397.1:n.-207+211_-207+230del | |
| ENST00000697687.1:n.191+55_191+74del | ||
| ENST00000697688.1:n.191+55_191+74del | ||
| ENST00000697689.1:c.*41_*60del | ENSP00000513398.1:n.*41_*60del | |
| ENST00000697690.1:c.145+55_145+74del | ENSP00000513399.1:n.145+55_145+74del | |
| ENST00000697691.1:c.42+158_42+177del | ENSP00000513400.1:n.42+158_42+177del | |
| ENST00000697692.1:c.*41_*60del | ENSP00000513401.1:n.*41_*60del | |
| ENST00000697693.1:n.113_132del | ||
| ENST00000337432.9:c.145+55_145+74del MANE Select | ENSP00000336701.4:n.145+55_145+74del | |
| ENST00000337432.8:c.145+55_145+74del | ENSP00000336701.4:n.145+55_145+74del | |
| ENST00000421782.3:c.145+55_145+74del | ENSP00000391450.2:n.145+55_145+74del | |
| ENST00000461271.5:c.-207+158_-207+177del | ENSP00000464056.1:n.-207+158_-207+177del | |
| ENST00000475762.5:c.*41_*60del | ENSP00000432421.1:n.*41_*60del | |
| ENST00000476741.2:n.187+55_187+74del | ||
| ENST00000482007.5:c.145+55_145+74del | ENSP00000433332.1:n.145+55_145+74del | |
| ENST00000486827.1:c.*41_*60del | ENSP00000436761.1:n.*41_*60del | |
| ENST00000487525.5:c.145+55_145+74del | ENSP00000431637.1:n.145+55_145+74del | |
| ENST00000487921.5:n.57+211_57+230del | ||
| ENST00000583539.5:c.145+55_145+74del | ENSP00000463121.1:n.145+55_145+74del | |
| ENST00000584617.5:c.126+55_126+74del | ||
| NM_002876.3:c.145+55_145+74del | NP_002867.1:n.145+55_145+74del | |
| NM_058216.2:c.145+55_145+74del | NP_478123.1:n.145+55_145+74del | |
| NR_103872.1:n.216+55_216+74del | ||
| NR_103873.1:n.113+158_113+177del | ||
| XM_006722001.2:c.145+55_145+74del | XP_006722064.1:n.145+55_145+74del | |
| XM_006722002.2:c.145+55_145+74del | XP_006722065.1:n.145+55_145+74del | |
| XM_006722004.2:c.-207+158_-207+177del | XP_006722067.1:n.-207+158_-207+177del | |
| XM_006722005.2:c.-207+211_-207+230del | XP_006722068.1:n.-207+211_-207+230del | |
| XM_011525092.1:c.-507+158_-507+177del | XP_011523394.1:n.-507+158_-507+177del | |
| XM_011525093.1:c.-668+158_-668+177del | XP_011523395.1:n.-668+158_-668+177del | |
| XM_011525094.1:c.-323_-304del | XP_011523396.1:n.-323_-304del | |
| XR_934513.1:n.218+55_218+74del | ||
| XR_934514.1:n.218+55_218+74del | ||
| XM_006722001.4:c.145+55_145+74del | XP_006722064.1:n.145+55_145+74del | |
| XM_006722002.4:c.145+55_145+74del | XP_006722065.1:n.145+55_145+74del | |
| XM_006722004.3:c.-207+158_-207+177del | XP_006722067.1:n.-207+158_-207+177del | |
| XM_006722005.3:c.-207+211_-207+230del | XP_006722068.1:n.-207+211_-207+230del | |
| XM_011525092.2:c.-507+158_-507+177del | XP_011523394.1:n.-507+158_-507+177del | |
| XM_011525093.2:c.-668+158_-668+177del | XP_011523395.1:n.-668+158_-668+177del | |
| XM_011525094.2:c.-323_-304del | XP_011523396.1:n.-323_-304del | |
| XM_017024914.1:c.-207+158_-207+177del | XP_016880403.1:n.-207+158_-207+177del | |
| XM_017024916.1:c.-507+158_-507+177del | XP_016880405.1:n.-507+158_-507+177del | |
| XM_017024917.1:c.-207+211_-207+230del | XP_016880406.1:n.-207+211_-207+230del | |
| XM_017024918.2:c.-323_-304del | XP_016880407.1:n.-323_-304del | |
| XM_017024919.1:c.-668+158_-668+177del | XP_016880408.1:n.-668+158_-668+177del | |
| XR_934513.3:n.649+55_649+74del | ||
| XR_934514.3:n.649+55_649+74del | ||
| NM_058216.3:c.145+55_145+74del MANE Select | NP_478123.1:n.145+55_145+74del | |
| NR_103872.2:n.187+55_187+74del | ||
| NM_002876.4:c.145+55_145+74del | NP_002867.1:n.145+55_145+74del |