Linked Data
ClinVar Variation Id:
1600605
ClinVar RCV Id:
RCV002118080
dbSNP Id:
rs537837939
ExAC:
14:58895199 GT / G
gnomAD v2:
14-58895199-GT-G
gnomAD v3:
14-58428481-GT-G
gnomAD v4:
14-58428481-GT-G
MyVariant Identifiers:
chr14:g.58895200del (hg19)
chr14:g.58428483del (hg38)
chr14:g.58428482del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.58428486del , CM000676.2:g.58428486del | GRCh38 |
| NC_000014.8:g.58895204del , CM000676.1:g.58895204del | GRCh37 |
| NC_000014.7:g.57964957del | NCBI36 |
| NG_051335.2:g.6102del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619722.5:c.-57+849del | ENSP00000481936.1:n.-57+849del | |
| ENST00000650845.1:n.745+23del | ||
| ENST00000650904.1:c.199+23del | ENSP00000498606.1:n.199+23del | |
| ENST00000651937.1:c.154+23del | ENSP00000498785.1:n.154+23del | |
| ENST00000652326.2:c.199+23del MANE Select | ENSP00000498929.1:n.199+23del | |
| ENST00000652732.1:c.-57+673del | ENSP00000498799.1:n.-57+673del | |
| ENST00000261244.9:c.199+23del | ENSP00000261244.5:n.199+23del | |
| ENST00000354386.10:c.235+23del | ENSP00000346359.6:n.235+23del | |
| ENST00000423743.7:c.-57+849del | ENSP00000399427.3:n.-57+849del | |
| ENST00000554463.5:c.-57+629del | ENSP00000451831.1:n.-57+629del | |
| ENST00000555203.5:c.-57+673del | ENSP00000452536.1:n.-57+673del | |
| ENST00000555833.5:c.-57+673del | ENSP00000450855.1:n.-57+673del | |
| ENST00000556134.5:c.-57+23del | ENSP00000452351.2:n.-57+23del | |
| ENST00000557192.1:n.92+673del | ||
| ENST00000619416.4:c.154+23del | ENSP00000478083.1:n.154+23del | |
| ENST00000619722.4:c.-57+849del | ENSP00000481936.1:n.-57+849del | |
| NM_001244189.1:c.235+23del | NP_001231118.1:n.235+23del | |
| NM_001244190.1:c.154+23del | NP_001231119.1:n.154+23del | |
| NM_001244191.1:c.-57+849del | NP_001231120.1:n.-57+849del | |
| NM_001244192.1:c.-57+849del | NP_001231121.1:n.-57+849del | |
| NM_014749.3:c.199+23del | NP_055564.3:n.199+23del | |
| NM_001329943.2:c.199+23del | NP_001316872.1:n.199+23del | |
| NM_001329944.1:c.199+23del | NP_001316873.1:n.199+23del | |
| NM_001329945.1:c.-57+673del | NP_001316874.1:n.-57+673del | |
| NM_001329946.1:c.199+23del | NP_001316875.1:n.199+23del | |
| NM_001329947.1:c.199+23del | NP_001316876.1:n.199+23del | |
| NM_001364700.1:c.-57+673del | NP_001351629.1:n.-57+673del | |
| NM_001364701.1:c.-57+673del | NP_001351630.1:n.-57+673del | |
| NM_014749.4:c.199+23del | NP_055564.3:n.199+23del | |
| XM_024449779.1:c.199+23del | XP_024305547.1:n.199+23del | |
| XM_024449780.1:c.199+23del | XP_024305548.1:n.199+23del | |
| XM_024449781.1:c.199+23del | XP_024305549.1:n.199+23del | |
| XM_024449782.1:c.-57+629del | XP_024305550.1:n.-57+629del | |
| XM_024449783.1:c.-57+673del | XP_024305551.1:n.-57+673del | |
| XM_024449784.1:c.-57+849del | XP_024305552.1:n.-57+849del | |
| XM_024449785.1:c.-57+673del | XP_024305553.1:n.-57+673del | |
| XM_024449791.1:c.199+23del | XP_024305559.1:n.199+23del | |
| NM_001244189.2:c.235+23del | NP_001231118.1:n.235+23del | |
| NM_001244190.2:c.154+23del | NP_001231119.1:n.154+23del | |
| NM_001244192.2:c.-57+849del | NP_001231121.1:n.-57+849del | |
| NM_001329943.3:c.199+23del MANE Select | NP_001316872.1:n.199+23del | |
| NM_001329944.2:c.199+23del | NP_001316873.1:n.199+23del | |
| NM_001329945.2:c.-57+673del | NP_001316874.1:n.-57+673del | |
| NM_001329946.2:c.199+23del | NP_001316875.1:n.199+23del | |
| NM_001329947.2:c.199+23del | NP_001316876.1:n.199+23del | |
| NM_001364701.2:c.-57+673del | NP_001351630.1:n.-57+673del | |
| NM_014749.5:c.199+23del | NP_055564.3:n.199+23del | |
| NM_001244191.2:c.-57+849del | NP_001231120.1:n.-57+849del |