Linked Data
dbSNP Id:
rs748472421
ExAC:
16:89805425 G / C
gnomAD v2:
16-89805425-G-C
gnomAD v3:
16-89739017-G-C
gnomAD v4:
16-89739017-G-C
MyVariant Identifiers:
chr16:g.89805425G>C (hg19)
chr16:g.89805425_89805426delinsCA (hg19)
chr16:g.89739017G>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89739017G>C , CM000678.2:g.89739017G>C | GRCh38 |
| NC_000016.9:g.89805425G>C , CM000678.1:g.89805425G>C | GRCh37 |
| NC_000016.8:g.88332926G>C | NCBI36 |
| NG_011706.1:g.82641C>G , LRG_495:g.82641C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561667.2:c.*2741-43C>G (FANCA) | ENSP00000512522.1:n.*2741-43C>G | |
| ENST00000564475.6:c.4172-43C>G (FANCA) | ENSP00000454977.2:n.4172-43C>G | |
| ENST00000567510.2:c.2742-43C>G (FANCA) | ENSP00000455969.1:n.2742-43C>G | |
| ENST00000568369.6:c.4172-43C>G (FANCA) | ENSP00000456829.1:n.4172-43C>G | |
| ENST00000696274.1:n.4129-43C>G (FANCA) | ||
| ENST00000696275.1:c.*3407-43C>G (FANCA) | ENSP00000512517.1:n.*3407-43C>G | |
| ENST00000696286.1:c.*81-43C>G (FANCA) | ENSP00000512523.1:n.*81-43C>G | |
| ENST00000696287.1:c.4043-43C>G (FANCA) | ENSP00000512524.1:n.4043-43C>G | |
| ENST00000696291.1:c.*3600-43C>G (FANCA) | ENSP00000512530.1:n.*3600-43C>G | |
| ENST00000389301.8:c.4168-43C>G (FANCA) MANE Select | ENSP00000373952.3:n.4168-43C>G | |
| ENST00000443381.7:c.*771G>C (ZNF276) MANE Select | ENSP00000415836.2:n.*771G>C | |
| ENST00000289816.9:c.*771G>C (ZNF276) | ENSP00000289816.5:n.*771G>C | |
| ENST00000389301.7:c.4168-43C>G (FANCA) | ENSP00000373952.3:n.4168-43C>G | |
| ENST00000561722.5:c.434C>G (FANCA) | ENSP00000456608.1:p.Ser145Cys | |
| ENST00000562424.1:n.439-43C>G (FANCA) | ||
| ENST00000563983.5:n.2604G>C (ZNF276) | ||
| ENST00000564475.5:c.502-43C>G (FANCA) | ||
| ENST00000564870.1:c.369-43C>G (FANCA) | ||
| ENST00000567879.5:c.542-43C>G (FANCA) | ENSP00000457006.1:n.542-43C>G | |
| ENST00000568369.5:c.4172-43C>G (FANCA) | ENSP00000456829.1:n.4172-43C>G | |
| NM_000135.2:c.4168-43C>G , LRG_495t1:c.4168-43C>G (FANCA) | NP_000126.2:n.4168-43C>G | |
| NM_001113525.1:c.*771G>C (ZNF276) | NP_001106997.1:n.*771G>C | |
| NM_001286167.1:c.4172-43C>G (FANCA) | NP_001273096.1:n.4172-43C>G | |
| NM_152287.3:c.*771G>C (ZNF276) | NP_689500.2:n.*771G>C | |
| NR_110122.1:n.2788G>C (ZNF276) | ||
| NR_110126.1:n.2671G>C (ZNF276) | ||
| NR_110128.1:n.2594G>C (ZNF276) | ||
| NR_110129.1:n.2683G>C (ZNF276) | ||
| XM_005256294.3:c.4172-43C>G (FANCA) | XP_005256351.1:n.4172-43C>G | |
| XM_011522945.1:c.4043-43C>G (FANCA) | XP_011521247.1:n.4043-43C>G | |
| XM_011522946.1:c.3149-43C>G (FANCA) | XP_011521248.1:n.3149-43C>G | |
| XM_011522947.1:c.3149-43C>G (FANCA) | XP_011521249.1:n.3149-43C>G | |
| XR_933244.1:n.4135-43C>G (FANCA) | ||
| XR_933245.1:n.4072-43C>G (FANCA) | ||
| NM_000135.3:c.4168-43C>G (FANCA) | NP_000126.2:n.4168-43C>G | |
| NM_001286167.2:c.4172-43C>G (FANCA) | NP_001273096.1:n.4172-43C>G | |
| XM_005256294.4:c.4172-43C>G (FANCA) | XP_005256351.1:n.4172-43C>G | |
| XM_011522945.2:c.4043-43C>G (FANCA) | XP_011521247.1:n.4043-43C>G | |
| XM_011522946.3:c.3149-43C>G (FANCA) | XP_011521248.1:n.3149-43C>G | |
| XM_011522947.2:c.3149-43C>G (FANCA) | XP_011521249.1:n.3149-43C>G | |
| XM_017023044.2:c.4039-43C>G (FANCA) | XP_016878533.1:n.4039-43C>G | |
| XM_017023890.1:c.*771G>C (ZNF276) | XP_016879379.1:n.*771G>C | |
| XM_024450189.1:c.3149-43C>G (FANCA) | XP_024305957.1:n.3149-43C>G | |
| XR_933244.2:n.4135-43C>G (FANCA) | ||
| XR_933245.2:n.4072-43C>G (FANCA) | ||
| XR_933484.2:n.2782G>C (ZNF276) | ||
| NM_000135.4:c.4168-43C>G (FANCA) MANE Select | NP_000126.2:n.4168-43C>G | |
| NM_001113525.2:c.*771G>C (ZNF276) MANE Select | NP_001106997.1:n.*771G>C | |
| NM_001286167.3:c.4172-43C>G (FANCA) | NP_001273096.1:n.4172-43C>G | |
| NM_152287.4:c.*771G>C (ZNF276) | NP_689500.2:n.*771G>C | |
| NR_110122.2:n.2771G>C (ZNF276) | ||
| NR_110126.2:n.2654G>C (ZNF276) | ||
| NR_110129.2:n.2688G>C (ZNF276) | ||
| NR_110128.2:n.2594G>C (ZNF276) |