Linked Data
ClinVar Variation Id:
408175
dbSNP Id:
rs149851163
ExAC:
16:89805351 C / T
gnomAD v2:
16-89805351-C-T
gnomAD v3:
16-89738943-C-T
gnomAD v4:
16-89738943-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89738943C>T , CM000678.2:g.89738943C>T | GRCh38 |
| NC_000016.9:g.89805351C>T , CM000678.1:g.89805351C>T | GRCh37 |
| NC_000016.8:g.88332852C>T | NCBI36 |
| NG_011706.1:g.82715G>A , LRG_495:g.82715G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561667.2:c.*2772G>A (FANCA) | ENSP00000512522.1:n.*2772G>A | |
| ENST00000564475.6:c.4203G>A (FANCA) | ENSP00000454977.2:p.Ser1401= | |
| ENST00000567510.2:c.2773G>A (FANCA) | ENSP00000455969.1:n.2773G>A | |
| ENST00000568369.6:c.4203G>A (FANCA) | ENSP00000456829.1:p.Ser1401= | |
| ENST00000696274.1:n.4160G>A (FANCA) | ||
| ENST00000696275.1:c.*3438G>A (FANCA) | ENSP00000512517.1:n.*3438G>A | |
| ENST00000696286.1:c.*112G>A (FANCA) | ENSP00000512523.1:n.*112G>A | |
| ENST00000696287.1:c.4074G>A (FANCA) | ENSP00000512524.1:p.Ser1358= | |
| ENST00000696291.1:c.*3631G>A (FANCA) | ENSP00000512530.1:n.*3631G>A | |
| ENST00000389301.8:c.4199G>A (FANCA) MANE Select | ENSP00000373952.3:p.Arg1400His | |
| ENST00000443381.7:c.*697C>T (ZNF276) MANE Select | ENSP00000415836.2:n.*697C>T | |
| ENST00000289816.9:c.*697C>T (ZNF276) | ENSP00000289816.5:n.*697C>T | |
| ENST00000389301.7:c.4199G>A (FANCA) | ENSP00000373952.3:p.Arg1400His | |
| ENST00000561722.5:c.436-17G>A (FANCA) | ENSP00000456608.1:n.436-17G>A | |
| ENST00000562424.1:n.470G>A (FANCA) | ||
| ENST00000563983.5:n.2530C>T (ZNF276) | ||
| ENST00000564475.5:c.533G>A (FANCA) | ||
| ENST00000564870.1:c.400G>A (FANCA) | ||
| ENST00000567879.5:c.573G>A (FANCA) | ENSP00000457006.1:p.Ser191= | |
| ENST00000568369.5:c.4203G>A (FANCA) | ENSP00000456829.1:p.Ser1401= | |
| NM_000135.2:c.4199G>A , LRG_495t1:c.4199G>A (FANCA) | NP_000126.2:p.Arg1400His | |
| NM_001113525.1:c.*697C>T (ZNF276) | NP_001106997.1:n.*697C>T | |
| NM_001286167.1:c.4203G>A (FANCA) | NP_001273096.1:p.Ser1401= | |
| NM_152287.3:c.*697C>T (ZNF276) | NP_689500.2:n.*697C>T | |
| NR_110122.1:n.2714C>T (ZNF276) | ||
| NR_110126.1:n.2597C>T (ZNF276) | ||
| NR_110128.1:n.2520C>T (ZNF276) | ||
| NR_110129.1:n.2609C>T (ZNF276) | ||
| XM_005256294.3:c.4203G>A (FANCA) | XP_005256351.1:p.Ser1401= | |
| XM_011522945.1:c.4074G>A (FANCA) | XP_011521247.1:p.Ser1358= | |
| XM_011522946.1:c.3180G>A (FANCA) | XP_011521248.1:p.Ser1060= | |
| XM_011522947.1:c.3180G>A (FANCA) | XP_011521249.1:p.Ser1060= | |
| XR_933244.1:n.4166G>A (FANCA) | ||
| XR_933245.1:n.4103G>A (FANCA) | ||
| NM_000135.3:c.4199G>A (FANCA) | NP_000126.2:p.Arg1400His | |
| NM_001286167.2:c.4203G>A (FANCA) | NP_001273096.1:p.Ser1401= | |
| XM_005256294.4:c.4203G>A (FANCA) | XP_005256351.1:p.Ser1401= | |
| XM_011522945.2:c.4074G>A (FANCA) | XP_011521247.1:p.Ser1358= | |
| XM_011522946.3:c.3180G>A (FANCA) | XP_011521248.1:p.Ser1060= | |
| XM_011522947.2:c.3180G>A (FANCA) | XP_011521249.1:p.Ser1060= | |
| XM_017023044.2:c.4070G>A (FANCA) | XP_016878533.1:p.Arg1357His | |
| XM_017023890.1:c.*697C>T (ZNF276) | XP_016879379.1:n.*697C>T | |
| XM_024450189.1:c.3180G>A (FANCA) | XP_024305957.1:p.Ser1060= | |
| XR_933244.2:n.4166G>A (FANCA) | ||
| XR_933245.2:n.4103G>A (FANCA) | ||
| XR_933484.2:n.2708C>T (ZNF276) | ||
| NM_000135.4:c.4199G>A (FANCA) MANE Select | NP_000126.2:p.Arg1400His | |
| NM_001113525.2:c.*697C>T (ZNF276) MANE Select | NP_001106997.1:n.*697C>T | |
| NM_001286167.3:c.4203G>A (FANCA) | NP_001273096.1:p.Ser1401= | |
| NM_152287.4:c.*697C>T (ZNF276) | NP_689500.2:n.*697C>T | |
| NR_110122.2:n.2697C>T (ZNF276) | ||
| NR_110126.2:n.2580C>T (ZNF276) | ||
| NR_110129.2:n.2614C>T (ZNF276) | ||
| NR_110128.2:n.2520C>T (ZNF276) |