Canonical Allele Identifier: CA8250573

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738644G>C , CM000678.2:g.89738644G>C	GRCh38
NC_000016.9:g.89805052G>C , CM000678.1:g.89805052G>C	GRCh37
NC_000016.8:g.88332553G>C	NCBI36
NG_011706.1:g.83014C>G , LRG_495:g.83014C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000135.4:c.4325C>G (FANCA) MANE Select	NP_000126.2:p.Ala1442Gly
NM_001113525.2:c.*398G>C (ZNF276) MANE Select	NP_001106997.1:n.*398G>C
ENST00000389301.8:c.4325C>G (FANCA) MANE Select	ENSP00000373952.3:p.Ala1442Gly
ENST00000443381.7:c.*398G>C (ZNF276) MANE Select	ENSP00000415836.2:n.*398G>C
NM_000135.2:c.4325C>G , LRG_495t1:c.4325C>G (FANCA)	NP_000126.2:p.Ala1442Gly
NM_000135.3:c.4325C>G (FANCA)	NP_000126.2:p.Ala1442Gly
NM_001113525.1:c.*398G>C (ZNF276)	NP_001106997.1:n.*398G>C
NM_001286167.1:c.*54C>G (FANCA)	NP_001273096.1:n.*54C>G
NM_001286167.2:c.*54C>G (FANCA)	NP_001273096.1:n.*54C>G
NM_001286167.3:c.*54C>G (FANCA)	NP_001273096.1:n.*54C>G
NM_152287.3:c.*398G>C (ZNF276)	NP_689500.2:n.*398G>C
NM_152287.4:c.*398G>C (ZNF276)	NP_689500.2:n.*398G>C
NR_110122.1:n.2415G>C (ZNF276)
NR_110122.2:n.2398G>C (ZNF276)
NR_110126.1:n.2298G>C (ZNF276)
NR_110126.2:n.2281G>C (ZNF276)
NR_110128.1:n.2221G>C (ZNF276)
NR_110128.2:n.2221G>C (ZNF276)
NR_110129.1:n.2310G>C (ZNF276)
NR_110129.2:n.2315G>C (ZNF276)
ENST00000289816.9:c.*398G>C (ZNF276)	ENSP00000289816.5:n.*398G>C
ENST00000389301.7:c.4325C>G (FANCA)	ENSP00000373952.3:p.Ala1442Gly
ENST00000561667.2:c.*3071C>G (FANCA)	ENSP00000512522.1:n.*3071C>G
ENST00000561722.5:c.545C>G (FANCA)	ENSP00000456608.1:p.Ala182Gly
ENST00000562424.1:n.596C>G (FANCA)
ENST00000563983.5:n.2231G>C (ZNF276)
ENST00000564475.6:c.*110C>G (FANCA)	ENSP00000454977.2:n.*110C>G
ENST00000567510.2:c.2899C>G (FANCA)	ENSP00000455969.1:n.2899C>G
ENST00000567879.5:c.699C>G (FANCA)	ENSP00000457006.1:n.699C>G
ENST00000568369.5:c.*54C>G (FANCA)	ENSP00000456829.1:n.*54C>G
ENST00000568369.6:c.*54C>G (FANCA)	ENSP00000456829.1:n.*54C>G
ENST00000696274.1:n.4459C>G (FANCA)
ENST00000696275.1:c.*3737C>G (FANCA)	ENSP00000512517.1:n.*3737C>G
ENST00000696286.1:c.*238C>G (FANCA)	ENSP00000512523.1:n.*238C>G
ENST00000696287.1:c.*110C>G (FANCA)	ENSP00000512524.1:n.*110C>G
ENST00000696291.1:c.*3930C>G (FANCA)	ENSP00000512530.1:n.*3930C>G
XM_005256294.4:c.*110C>G (FANCA)	XP_005256351.1:n.*110C>G
XM_011522945.2:c.*110C>G (FANCA)	XP_011521247.1:n.*110C>G
XM_011522946.3:c.*110C>G (FANCA)	XP_011521248.1:n.*110C>G
XM_011522947.2:c.*110C>G (FANCA)	XP_011521249.1:n.*110C>G
XM_017023044.2:c.4196C>G (FANCA)	XP_016878533.1:p.Ala1399Gly
XM_017023890.1:c.*398G>C (ZNF276)	XP_016879379.1:n.*398G>C
XM_024450189.1:c.*110C>G (FANCA)	XP_024305957.1:n.*110C>G
XR_933244.1:n.4292C>G (FANCA)
XR_933244.2:n.4292C>G (FANCA)
XR_933245.1:n.4229C>G (FANCA)
XR_933245.2:n.4229C>G (FANCA)
XR_933484.2:n.2409G>C (ZNF276)