Canonical Allele Identifier: CA10649305

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738315G>A , CM000678.2:g.89738315G>A	GRCh38
NC_000016.9:g.89804723G>A , CM000678.1:g.89804723G>A	GRCh37
NC_000016.8:g.88332224G>A	NCBI36
NG_011706.1:g.83343C>T , LRG_495:g.83343C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*3400C>T (FANCA)	ENSP00000512522.1:n.*3400C>T
ENST00000568369.6:c.*383C>T (FANCA)	ENSP00000456829.1:n.*383C>T
ENST00000389301.8:c.*286C>T (FANCA) MANE Select	ENSP00000373952.3:n.*286C>T
ENST00000443381.7:c.*69G>A (ZNF276) MANE Select	ENSP00000415836.2:n.*69G>A
ENST00000289816.9:c.*69G>A (ZNF276)	ENSP00000289816.5:n.*69G>A
ENST00000389301.7:c.*286C>T (FANCA)	ENSP00000373952.3:n.*286C>T
ENST00000443381.6:c.*69G>A (ZNF276)	ENSP00000415836.2:n.*69G>A
ENST00000561536.5:n.1673G>A (ZNF276)
ENST00000563983.5:n.1902G>A (ZNF276)
ENST00000564004.5:n.2590G>A (ZNF276)
ENST00000568064.5:c.*406G>A (ZNF276)	ENSP00000457210.1:n.*406G>A
ENST00000568295.5:c.*814G>A (ZNF276)	ENSP00000457313.1:n.*814G>A
ENST00000569901.1:n.534G>A (ZNF276)
NM_000135.2:c.*286C>T , LRG_495t1:c.*286C>T (FANCA)	NP_000126.2:n.*286C>T
NM_001113525.1:c.*69G>A (ZNF276)	NP_001106997.1:n.*69G>A
NM_001286167.1:c.*383C>T (FANCA)	NP_001273096.1:n.*383C>T
NM_152287.3:c.*69G>A (ZNF276)	NP_689500.2:n.*69G>A
NR_110122.1:n.2086G>A (ZNF276)
NR_110126.1:n.1969G>A (ZNF276)
NR_110128.1:n.1892G>A (ZNF276)
NR_110129.1:n.1981G>A (ZNF276)
XM_005256324.3:c.*69G>A (ZNF276)	XP_005256381.1:n.*69G>A
XM_005256328.3:c.*69G>A (ZNF276)	XP_005256385.1:n.*69G>A
XM_006721337.1:c.*69G>A (ZNF276)	XP_006721400.1:n.*69G>A
XM_011523460.1:c.*69G>A (ZNF276)	XP_011521762.1:n.*69G>A
XR_429740.1:n.2096G>A (ZNF276)
NM_000135.3:c.*286C>T (FANCA)	NP_000126.2:n.*286C>T
NM_001286167.2:c.*383C>T (FANCA)	NP_001273096.1:n.*383C>T
XM_017023890.1:c.*69G>A (ZNF276)	XP_016879379.1:n.*69G>A
XR_001752030.1:n.3133G>A (ZNF276)
XR_001752031.1:n.2077G>A (ZNF276)
XR_002957853.1:n.2493G>A (ZNF276)
XR_243507.2:n.1992G>A (ZNF276)
XR_429740.2:n.2096G>A (ZNF276)
XR_933484.2:n.2080G>A (ZNF276)
NM_000135.4:c.*286C>T (FANCA) MANE Select	NP_000126.2:n.*286C>T
NM_001113525.2:c.*69G>A (ZNF276) MANE Select	NP_001106997.1:n.*69G>A
NM_001286167.3:c.*383C>T (FANCA)	NP_001273096.1:n.*383C>T
NM_152287.4:c.*69G>A (ZNF276)	NP_689500.2:n.*69G>A
NR_110122.2:n.2069G>A (ZNF276)
NR_110126.2:n.1952G>A (ZNF276)
NR_110129.2:n.1986G>A (ZNF276)
NR_110128.2:n.1892G>A (ZNF276)