Canonical Allele Identifier: CA2580092322

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89740803del , CM000678.2:g.89740803del	GRCh38
NC_000016.9:g.89807211del , CM000678.1:g.89807211del	GRCh37
NC_000016.8:g.88334712del	NCBI36
NG_011706.1:g.80855del , LRG_495:g.80855del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2306+1del (FANCA)	ENSP00000512522.1:n.*2306+1del
ENST00000564475.6:c.3828+1del (FANCA)	ENSP00000454977.2:n.3828+1del
ENST00000567510.2:c.2398+1del (FANCA)	ENSP00000455969.1:n.2398+1del
ENST00000568369.6:c.3828+1del (FANCA)	ENSP00000456829.1:n.3828+1del
ENST00000696274.1:n.3789+1del (FANCA)
ENST00000696275.1:c.*3063+1del (FANCA)	ENSP00000512517.1:n.*3063+1del
ENST00000696286.1:c.3828+1del (FANCA)	ENSP00000512523.1:n.3828+1del
ENST00000696287.1:c.3699+1del (FANCA)	ENSP00000512524.1:n.3699+1del
ENST00000696291.1:c.*3260+1del (FANCA)	ENSP00000512530.1:n.*3260+1del
ENST00000389301.8:c.3828+1del (FANCA) MANE Select	ENSP00000373952.3:n.3828+1del
ENST00000443381.7:c.*2557del (ZNF276) MANE Select	ENSP00000415836.2:n.*2557del
ENST00000289816.9:c.*2557del (ZNF276)	ENSP00000289816.5:n.*2557del
ENST00000305699.15:n.1071+1del (FANCA)
ENST00000389301.7:c.3828+1del (FANCA)	ENSP00000373952.3:n.3828+1del
ENST00000564475.5:c.158+1del (FANCA)
ENST00000564870.1:c.30-704del (FANCA)
ENST00000564969.5:n.113+1del (FANCA)
ENST00000567879.5:c.306+1del (FANCA)	ENSP00000457006.1:n.306+1del
ENST00000568369.5:c.3828+1del (FANCA)	ENSP00000456829.1:n.3828+1del
ENST00000568626.1:c.537+1del (FANCA)
NM_000135.2:c.3828+1del , LRG_495t1:c.3828+1del (FANCA)	NP_000126.2:n.3828+1del
NM_001113525.1:c.*2557del (ZNF276)	NP_001106997.1:n.*2557del
NM_001286167.1:c.3828+1del (FANCA)	NP_001273096.1:n.3828+1del
NM_152287.3:c.*2557del (ZNF276)	NP_689500.2:n.*2557del
XM_005256294.3:c.3828+1del (FANCA)	XP_005256351.1:n.3828+1del
XM_011522945.1:c.3699+1del (FANCA)	XP_011521247.1:n.3699+1del
XM_011522946.1:c.2805+1del (FANCA)	XP_011521248.1:n.2805+1del
XM_011522947.1:c.2805+1del (FANCA)	XP_011521249.1:n.2805+1del
XR_933244.1:n.3871+1del (FANCA)
XR_933245.1:n.3732+1del (FANCA)
XR_933246.1:n.3698+1del (FANCA)
NM_000135.3:c.3828+1del (FANCA)	NP_000126.2:n.3828+1del
NM_001286167.2:c.3828+1del (FANCA)	NP_001273096.1:n.3828+1del
XM_005256294.4:c.3828+1del (FANCA)	XP_005256351.1:n.3828+1del
XM_011522945.2:c.3699+1del (FANCA)	XP_011521247.1:n.3699+1del
XM_011522946.3:c.2805+1del (FANCA)	XP_011521248.1:n.2805+1del
XM_011522947.2:c.2805+1del (FANCA)	XP_011521249.1:n.2805+1del
XM_017023044.2:c.3699+1del (FANCA)	XP_016878533.1:n.3699+1del
XM_024450189.1:c.2805+1del (FANCA)	XP_024305957.1:n.2805+1del
XR_001751866.1:n.3698+1del (FANCA)
XR_933244.2:n.3871+1del (FANCA)
XR_933245.2:n.3732+1del (FANCA)
NM_000135.4:c.3828+1del (FANCA) MANE Select	NP_000126.2:n.3828+1del
NM_001113525.2:c.*2557del (ZNF276) MANE Select	NP_001106997.1:n.*2557del
NM_001286167.3:c.3828+1del (FANCA)	NP_001273096.1:n.3828+1del
NM_152287.4:c.*2557del (ZNF276)	NP_689500.2:n.*2557del
NR_110122.2:n.4557del (ZNF276)
NR_110126.2:n.4440del (ZNF276)
NR_110129.2:n.4474del (ZNF276)
NR_110128.2:n.4380del (ZNF276)