Linked Data
dbSNP Id:
rs772262735
ExAC:
16:89805986 G / A
gnomAD v2:
16-89805986-G-A
gnomAD v3:
16-89739578-G-A
gnomAD v4:
16-89739578-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89739578G>A , CM000678.2:g.89739578G>A | GRCh38 |
| NC_000016.9:g.89805986G>A , CM000678.1:g.89805986G>A | GRCh37 |
| NC_000016.8:g.88333487G>A | NCBI36 |
| NG_011706.1:g.82080C>T , LRG_495:g.82080C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561667.2:c.*2508-25C>T (FANCA) | ENSP00000512522.1:n.*2508-25C>T | |
| ENST00000564475.6:c.3935-25C>T (FANCA) | ENSP00000454977.2:n.3935-25C>T | |
| ENST00000567510.2:c.2505-25C>T (FANCA) | ENSP00000455969.1:n.2505-25C>T | |
| ENST00000568369.6:c.3935-25C>T (FANCA) | ENSP00000456829.1:n.3935-25C>T | |
| ENST00000696274.1:n.3896-25C>T (FANCA) | ||
| ENST00000696275.1:c.*3170-25C>T (FANCA) | ENSP00000512517.1:n.*3170-25C>T | |
| ENST00000696286.1:c.3935-289C>T (FANCA) | ENSP00000512523.1:n.3935-289C>T | |
| ENST00000696287.1:c.3806-25C>T (FANCA) | ENSP00000512524.1:n.3806-25C>T | |
| ENST00000696291.1:c.*3367-25C>T (FANCA) | ENSP00000512530.1:n.*3367-25C>T | |
| ENST00000389301.8:c.3935-25C>T (FANCA) MANE Select | ENSP00000373952.3:n.3935-25C>T | |
| ENST00000443381.7:c.*1332G>A (ZNF276) MANE Select | ENSP00000415836.2:n.*1332G>A | |
| ENST00000289816.9:c.*1332G>A (ZNF276) | ENSP00000289816.5:n.*1332G>A | |
| ENST00000389301.7:c.3935-25C>T (FANCA) | ENSP00000373952.3:n.3935-25C>T | |
| ENST00000561722.5:c.86-25C>T (FANCA) | ENSP00000456608.1:n.86-25C>T | |
| ENST00000562424.1:n.181C>T (FANCA) | ||
| ENST00000563983.5:n.3165G>A (ZNF276) | ||
| ENST00000564475.5:c.265-25C>T (FANCA) | ||
| ENST00000564870.1:c.136-25C>T (FANCA) | ||
| ENST00000564969.5:n.635C>T (FANCA) | ||
| ENST00000567879.5:c.413-312C>T (FANCA) | ENSP00000457006.1:n.413-312C>T | |
| ENST00000568369.5:c.3935-25C>T (FANCA) | ENSP00000456829.1:n.3935-25C>T | |
| ENST00000568626.1:c.644-25C>T (FANCA) | ||
| NM_000135.2:c.3935-25C>T , LRG_495t1:c.3935-25C>T (FANCA) | NP_000126.2:n.3935-25C>T | |
| NM_001113525.1:c.*1332G>A (ZNF276) | NP_001106997.1:n.*1332G>A | |
| NM_001286167.1:c.3935-25C>T (FANCA) | NP_001273096.1:n.3935-25C>T | |
| NM_152287.3:c.*1332G>A (ZNF276) | NP_689500.2:n.*1332G>A | |
| NR_110122.1:n.3349G>A (ZNF276) | ||
| NR_110126.1:n.3232G>A (ZNF276) | ||
| NR_110128.1:n.3155G>A (ZNF276) | ||
| NR_110129.1:n.3244G>A (ZNF276) | ||
| XM_005256294.3:c.3935-25C>T (FANCA) | XP_005256351.1:n.3935-25C>T | |
| XM_011522945.1:c.3806-25C>T (FANCA) | XP_011521247.1:n.3806-25C>T | |
| XM_011522946.1:c.2912-25C>T (FANCA) | XP_011521248.1:n.2912-25C>T | |
| XM_011522947.1:c.2912-25C>T (FANCA) | XP_011521249.1:n.2912-25C>T | |
| XR_933244.1:n.3978-289C>T (FANCA) | ||
| XR_933245.1:n.3839-25C>T (FANCA) | ||
| NM_000135.3:c.3935-25C>T (FANCA) | NP_000126.2:n.3935-25C>T | |
| NM_001286167.2:c.3935-25C>T (FANCA) | NP_001273096.1:n.3935-25C>T | |
| XM_005256294.4:c.3935-25C>T (FANCA) | XP_005256351.1:n.3935-25C>T | |
| XM_011522945.2:c.3806-25C>T (FANCA) | XP_011521247.1:n.3806-25C>T | |
| XM_011522946.3:c.2912-25C>T (FANCA) | XP_011521248.1:n.2912-25C>T | |
| XM_011522947.2:c.2912-25C>T (FANCA) | XP_011521249.1:n.2912-25C>T | |
| XM_017023044.2:c.3806-25C>T (FANCA) | XP_016878533.1:n.3806-25C>T | |
| XM_017023890.1:c.*1332G>A (ZNF276) | XP_016879379.1:n.*1332G>A | |
| XM_024450189.1:c.2912-25C>T (FANCA) | XP_024305957.1:n.2912-25C>T | |
| XR_001751866.1:n.3805-25C>T (FANCA) | ||
| XR_933244.2:n.3978-289C>T (FANCA) | ||
| XR_933245.2:n.3839-25C>T (FANCA) | ||
| XR_933484.2:n.3343G>A (ZNF276) | ||
| NM_000135.4:c.3935-25C>T (FANCA) MANE Select | NP_000126.2:n.3935-25C>T | |
| NM_001113525.2:c.*1332G>A (ZNF276) MANE Select | NP_001106997.1:n.*1332G>A | |
| NM_001286167.3:c.3935-25C>T (FANCA) | NP_001273096.1:n.3935-25C>T | |
| NM_152287.4:c.*1332G>A (ZNF276) | NP_689500.2:n.*1332G>A | |
| NR_110122.2:n.3332G>A (ZNF276) | ||
| NR_110126.2:n.3215G>A (ZNF276) | ||
| NR_110129.2:n.3249G>A (ZNF276) | ||
| NR_110128.2:n.3155G>A (ZNF276) |