Canonical Allele Identifier: CA286613581

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738492G>A , CM000678.2:g.89738492G>A	GRCh38
NC_000016.9:g.89804900G>A , CM000678.1:g.89804900G>A	GRCh37
NC_000016.8:g.88332401G>A	NCBI36
NG_011706.1:g.83166C>T , LRG_495:g.83166C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000135.4:c.*109C>T (FANCA) MANE Select	NP_000126.2:n.*109C>T
NM_001113525.2:c.*246G>A (ZNF276) MANE Select	NP_001106997.1:n.*246G>A
ENST00000389301.8:c.*109C>T (FANCA) MANE Select	ENSP00000373952.3:n.*109C>T
ENST00000443381.7:c.*246G>A (ZNF276) MANE Select	ENSP00000415836.2:n.*246G>A
NM_000135.2:c.*109C>T , LRG_495t1:c.*109C>T (FANCA)	NP_000126.2:n.*109C>T
NM_000135.3:c.*109C>T (FANCA)	NP_000126.2:n.*109C>T
NM_001113525.1:c.*246G>A (ZNF276)	NP_001106997.1:n.*246G>A
NM_001286167.1:c.*206C>T (FANCA)	NP_001273096.1:n.*206C>T
NM_001286167.2:c.*206C>T (FANCA)	NP_001273096.1:n.*206C>T
NM_001286167.3:c.*206C>T (FANCA)	NP_001273096.1:n.*206C>T
NM_152287.3:c.*246G>A (ZNF276)	NP_689500.2:n.*246G>A
NM_152287.4:c.*246G>A (ZNF276)	NP_689500.2:n.*246G>A
NR_110122.1:n.2263G>A (ZNF276)
NR_110122.2:n.2246G>A (ZNF276)
NR_110126.1:n.2146G>A (ZNF276)
NR_110126.2:n.2129G>A (ZNF276)
NR_110128.1:n.2069G>A (ZNF276)
NR_110128.2:n.2069G>A (ZNF276)
NR_110129.1:n.2158G>A (ZNF276)
NR_110129.2:n.2163G>A (ZNF276)
ENST00000289816.9:c.*246G>A (ZNF276)	ENSP00000289816.5:n.*246G>A
ENST00000389301.7:c.*109C>T (FANCA)	ENSP00000373952.3:n.*109C>T
ENST00000443381.6:c.*246G>A (ZNF276)	ENSP00000415836.2:n.*246G>A
ENST00000561536.5:n.1850G>A (ZNF276)
ENST00000561667.2:c.*3223C>T (FANCA)	ENSP00000512522.1:n.*3223C>T
ENST00000563983.5:n.2079G>A (ZNF276)
ENST00000564004.5:n.2767G>A (ZNF276)
ENST00000568064.5:c.*583G>A (ZNF276)	ENSP00000457210.1:n.*583G>A
ENST00000568295.5:c.*991G>A (ZNF276)	ENSP00000457313.1:n.*991G>A
ENST00000568369.5:c.*206C>T (FANCA)	ENSP00000456829.1:n.*206C>T
ENST00000568369.6:c.*206C>T (FANCA)	ENSP00000456829.1:n.*206C>T
XM_005256324.3:c.*246G>A (ZNF276)	XP_005256381.1:n.*246G>A
XM_005256328.3:c.*246G>A (ZNF276)	XP_005256385.1:n.*246G>A
XM_006721337.1:c.*246G>A (ZNF276)	XP_006721400.1:n.*246G>A
XM_011523460.1:c.*246G>A (ZNF276)	XP_011521762.1:n.*246G>A
XM_017023044.2:c.*109C>T (FANCA)	XP_016878533.1:n.*109C>T
XM_017023890.1:c.*246G>A (ZNF276)	XP_016879379.1:n.*246G>A
XR_001752030.1:n.3310G>A (ZNF276)
XR_001752031.1:n.2254G>A (ZNF276)
XR_002957853.1:n.2670G>A (ZNF276)
XR_243507.2:n.2169G>A (ZNF276)
XR_429740.2:n.2273G>A (ZNF276)
XR_933244.2:n.4444C>T (FANCA)
XR_933484.2:n.2257G>A (ZNF276)