Linked Data
ClinVar Variation Id:
2049844
dbSNP Id:
rs1177499044
gnomAD v2:
16-89805357-T-C
gnomAD v4:
16-89738949-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89738949T>C , CM000678.2:g.89738949T>C | GRCh38 |
| NC_000016.9:g.89805357T>C , CM000678.1:g.89805357T>C | GRCh37 |
| NC_000016.8:g.88332858T>C | NCBI36 |
| NG_011706.1:g.82709A>G , LRG_495:g.82709A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561667.2:c.*2766A>G (FANCA) | ENSP00000512522.1:n.*2766A>G | |
| ENST00000564475.6:c.4197A>G (FANCA) | ENSP00000454977.2:p.Lys1399= | |
| ENST00000567510.2:c.2767A>G (FANCA) | ENSP00000455969.1:n.2767A>G | |
| ENST00000568369.6:c.4197A>G (FANCA) | ENSP00000456829.1:p.Lys1399= | |
| ENST00000696274.1:n.4154A>G (FANCA) | ||
| ENST00000696275.1:c.*3432A>G (FANCA) | ENSP00000512517.1:n.*3432A>G | |
| ENST00000696286.1:c.*106A>G (FANCA) | ENSP00000512523.1:n.*106A>G | |
| ENST00000696287.1:c.4068A>G (FANCA) | ENSP00000512524.1:p.Lys1356= | |
| ENST00000696291.1:c.*3625A>G (FANCA) | ENSP00000512530.1:n.*3625A>G | |
| ENST00000389301.8:c.4193A>G (FANCA) MANE Select | ENSP00000373952.3:p.Lys1398Arg | |
| ENST00000443381.7:c.*703T>C (ZNF276) MANE Select | ENSP00000415836.2:n.*703T>C | |
| ENST00000289816.9:c.*703T>C (ZNF276) | ENSP00000289816.5:n.*703T>C | |
| ENST00000389301.7:c.4193A>G (FANCA) | ENSP00000373952.3:p.Lys1398Arg | |
| ENST00000561722.5:c.436-23A>G (FANCA) | ENSP00000456608.1:n.436-23A>G | |
| ENST00000562424.1:n.464A>G (FANCA) | ||
| ENST00000563983.5:n.2536T>C (ZNF276) | ||
| ENST00000564475.5:c.527A>G (FANCA) | ||
| ENST00000564870.1:c.394A>G (FANCA) | ||
| ENST00000567879.5:c.567A>G (FANCA) | ENSP00000457006.1:p.Lys189= | |
| ENST00000568369.5:c.4197A>G (FANCA) | ENSP00000456829.1:p.Lys1399= | |
| NM_000135.2:c.4193A>G , LRG_495t1:c.4193A>G (FANCA) | NP_000126.2:p.Lys1398Arg | |
| NM_001113525.1:c.*703T>C (ZNF276) | NP_001106997.1:n.*703T>C | |
| NM_001286167.1:c.4197A>G (FANCA) | NP_001273096.1:p.Lys1399= | |
| NM_152287.3:c.*703T>C (ZNF276) | NP_689500.2:n.*703T>C | |
| NR_110122.1:n.2720T>C (ZNF276) | ||
| NR_110126.1:n.2603T>C (ZNF276) | ||
| NR_110128.1:n.2526T>C (ZNF276) | ||
| NR_110129.1:n.2615T>C (ZNF276) | ||
| XM_005256294.3:c.4197A>G (FANCA) | XP_005256351.1:p.Lys1399= | |
| XM_011522945.1:c.4068A>G (FANCA) | XP_011521247.1:p.Lys1356= | |
| XM_011522946.1:c.3174A>G (FANCA) | XP_011521248.1:p.Lys1058= | |
| XM_011522947.1:c.3174A>G (FANCA) | XP_011521249.1:p.Lys1058= | |
| XR_933244.1:n.4160A>G (FANCA) | ||
| XR_933245.1:n.4097A>G (FANCA) | ||
| NM_000135.3:c.4193A>G (FANCA) | NP_000126.2:p.Lys1398Arg | |
| NM_001286167.2:c.4197A>G (FANCA) | NP_001273096.1:p.Lys1399= | |
| XM_005256294.4:c.4197A>G (FANCA) | XP_005256351.1:p.Lys1399= | |
| XM_011522945.2:c.4068A>G (FANCA) | XP_011521247.1:p.Lys1356= | |
| XM_011522946.3:c.3174A>G (FANCA) | XP_011521248.1:p.Lys1058= | |
| XM_011522947.2:c.3174A>G (FANCA) | XP_011521249.1:p.Lys1058= | |
| XM_017023044.2:c.4064A>G (FANCA) | XP_016878533.1:p.Lys1355Arg | |
| XM_017023890.1:c.*703T>C (ZNF276) | XP_016879379.1:n.*703T>C | |
| XM_024450189.1:c.3174A>G (FANCA) | XP_024305957.1:p.Lys1058= | |
| XR_933244.2:n.4160A>G (FANCA) | ||
| XR_933245.2:n.4097A>G (FANCA) | ||
| XR_933484.2:n.2714T>C (ZNF276) | ||
| NM_000135.4:c.4193A>G (FANCA) MANE Select | NP_000126.2:p.Lys1398Arg | |
| NM_001113525.2:c.*703T>C (ZNF276) MANE Select | NP_001106997.1:n.*703T>C | |
| NM_001286167.3:c.4197A>G (FANCA) | NP_001273096.1:p.Lys1399= | |
| NM_152287.4:c.*703T>C (ZNF276) | NP_689500.2:n.*703T>C | |
| NR_110122.2:n.2703T>C (ZNF276) | ||
| NR_110126.2:n.2586T>C (ZNF276) | ||
| NR_110129.2:n.2620T>C (ZNF276) | ||
| NR_110128.2:n.2526T>C (ZNF276) |