Canonical Allele Identifier: CA2573152883

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738853_89738876del , CM000678.2:g.89738853_89738876del	GRCh38
NC_000016.9:g.89805261_89805284del , CM000678.1:g.89805261_89805284del	GRCh37
NC_000016.8:g.88332762_88332785del	NCBI36
NG_011706.1:g.82784_82807del , LRG_495:g.82784_82807del

Transcript Alleles

HGVS	Amino-acid Change
NM_000135.4:c.4260+8_4260+31del (FANCA) MANE Select	NP_000126.2:n.4260+8_4260+31del
NM_001113525.2:c.*607_*630del (ZNF276) MANE Select	NP_001106997.1:n.*607_*630del
ENST00000389301.8:c.4260+8_4260+31del (FANCA) MANE Select	ENSP00000373952.3:n.4260+8_4260+31del
ENST00000443381.7:c.*607_*630del (ZNF276) MANE Select	ENSP00000415836.2:n.*607_*630del
NM_000135.2:c.4260+8_4260+31del , LRG_495t1:c.4260+8_4260+31del (FANCA)	NP_000126.2:n.4260+8_4260+31del
NM_000135.3:c.4260+8_4260+31del (FANCA)	NP_000126.2:n.4260+8_4260+31del
NM_001113525.1:c.*607_*630del (ZNF276)	NP_001106997.1:n.*607_*630del
NM_001286167.1:c.4264+8_4264+31del (FANCA)	NP_001273096.1:n.4264+8_4264+31del
NM_001286167.2:c.4264+8_4264+31del (FANCA)	NP_001273096.1:n.4264+8_4264+31del
NM_001286167.3:c.4264+8_4264+31del (FANCA)	NP_001273096.1:n.4264+8_4264+31del
NM_152287.3:c.*607_*630del (ZNF276)	NP_689500.2:n.*607_*630del
NM_152287.4:c.*607_*630del (ZNF276)	NP_689500.2:n.*607_*630del
NR_110122.1:n.2624_2647del (ZNF276)
NR_110122.2:n.2607_2630del (ZNF276)
NR_110126.1:n.2507_2530del (ZNF276)
NR_110126.2:n.2490_2513del (ZNF276)
NR_110128.1:n.2430_2453del (ZNF276)
NR_110128.2:n.2430_2453del (ZNF276)
NR_110129.1:n.2519_2542del (ZNF276)
NR_110129.2:n.2524_2547del (ZNF276)
ENST00000289816.9:c.*607_*630del (ZNF276)	ENSP00000289816.5:n.*607_*630del
ENST00000389301.7:c.4260+8_4260+31del (FANCA)	ENSP00000373952.3:n.4260+8_4260+31del
ENST00000561667.2:c.*2841_*2864del (FANCA)	ENSP00000512522.1:n.*2841_*2864del
ENST00000561722.5:c.480+8_480+31del (FANCA)	ENSP00000456608.1:n.480+8_480+31del
ENST00000562424.1:n.531+8_531+31del (FANCA)
ENST00000563983.5:n.2440_2463del (ZNF276)
ENST00000564475.5:c.602_625del (FANCA)
ENST00000564475.6:c.4272_4295del (FANCA)	ENSP00000454977.2:p.Lys1425_Val1432del
ENST00000567510.2:c.2834+8_2834+31del (FANCA)	ENSP00000455969.1:n.2834+8_2834+31del
ENST00000567879.5:c.634+8_634+31del (FANCA)	ENSP00000457006.1:n.634+8_634+31del
ENST00000568369.5:c.4264+8_4264+31del (FANCA)	ENSP00000456829.1:n.4264+8_4264+31del
ENST00000568369.6:c.4264+8_4264+31del (FANCA)	ENSP00000456829.1:n.4264+8_4264+31del
ENST00000696274.1:n.4229_4252del (FANCA)
ENST00000696275.1:c.*3507_*3530del (FANCA)	ENSP00000512517.1:n.*3507_*3530del
ENST00000696286.1:c.*173+8_*173+31del (FANCA)	ENSP00000512523.1:n.*173+8_*173+31del
ENST00000696287.1:c.4143_4166del (FANCA)	ENSP00000512524.1:p.Lys1382_Val1389del
ENST00000696291.1:c.*3700_*3723del (FANCA)	ENSP00000512530.1:n.*3700_*3723del
XM_005256294.3:c.4272_4295del (FANCA)	XP_005256351.1:p.Lys1425_Val1432del
XM_005256294.4:c.4272_4295del (FANCA)	XP_005256351.1:p.Lys1425_Val1432del
XM_011522945.1:c.4143_4166del (FANCA)	XP_011521247.1:p.Lys1382_Val1389del
XM_011522945.2:c.4143_4166del (FANCA)	XP_011521247.1:p.Lys1382_Val1389del
XM_011522946.1:c.3249_3272del (FANCA)	XP_011521248.1:p.Lys1084_Val1091del
XM_011522946.3:c.3249_3272del (FANCA)	XP_011521248.1:p.Lys1084_Val1091del
XM_011522947.1:c.3249_3272del (FANCA)	XP_011521249.1:p.Lys1084_Val1091del
XM_011522947.2:c.3249_3272del (FANCA)	XP_011521249.1:p.Lys1084_Val1091del
XM_017023044.2:c.4131+8_4131+31del (FANCA)	XP_016878533.1:n.4131+8_4131+31del
XM_017023890.1:c.*607_*630del (ZNF276)	XP_016879379.1:n.*607_*630del
XM_024450189.1:c.3249_3272del (FANCA)	XP_024305957.1:p.Lys1084_Val1091del
XR_933244.1:n.4227+8_4227+31del (FANCA)
XR_933244.2:n.4227+8_4227+31del (FANCA)
XR_933245.1:n.4164+8_4164+31del (FANCA)
XR_933245.2:n.4164+8_4164+31del (FANCA)
XR_933484.2:n.2618_2641del (ZNF276)