Canonical Allele Identifier: CA8250426

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89737922A>C , CM000678.2:g.89737922A>C	GRCh38
NC_000016.9:g.89804330A>C , CM000678.1:g.89804330A>C	GRCh37
NC_000016.8:g.88331831A>C	NCBI36
NG_011706.1:g.83736T>G , LRG_495:g.83736T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000135.4:c.*679T>G (FANCA) MANE Select	NP_000126.2:n.*679T>G
NM_001113525.2:c.1574+17A>C (ZNF276) MANE Select	NP_001106997.1:n.1574+17A>C
ENST00000389301.8:c.*679T>G (FANCA) MANE Select	ENSP00000373952.3:n.*679T>G
ENST00000443381.7:c.1574+17A>C (ZNF276) MANE Select	ENSP00000415836.2:n.1574+17A>C
NM_000135.2:c.*679T>G , LRG_495t1:c.*679T>G (FANCA)	NP_000126.2:n.*679T>G
NM_000135.3:c.*679T>G (FANCA)	NP_000126.2:n.*679T>G
NM_001113525.1:c.1574+17A>C (ZNF276)	NP_001106997.1:n.1574+17A>C
NM_001286167.1:c.*776T>G (FANCA)	NP_001273096.1:n.*776T>G
NM_001286167.2:c.*776T>G (FANCA)	NP_001273096.1:n.*776T>G
NM_001286167.3:c.*776T>G (FANCA)	NP_001273096.1:n.*776T>G
NM_152287.3:c.1349+17A>C (ZNF276)	NP_689500.2:n.1349+17A>C
NM_152287.4:c.1349+17A>C (ZNF276)	NP_689500.2:n.1349+17A>C
NR_110122.1:n.1746+17A>C (ZNF276)
NR_110122.2:n.1729+17A>C (ZNF276)
NR_110126.1:n.1629+17A>C (ZNF276)
NR_110126.2:n.1612+17A>C (ZNF276)
NR_110128.1:n.1552+17A>C (ZNF276)
NR_110128.2:n.1552+17A>C (ZNF276)
NR_110129.1:n.1641+17A>C (ZNF276)
NR_110129.2:n.1646+17A>C (ZNF276)
ENST00000289816.9:c.1349+17A>C (ZNF276)	ENSP00000289816.5:n.1349+17A>C
ENST00000389301.7:c.*679T>G (FANCA)	ENSP00000373952.3:n.*679T>G
ENST00000443381.6:c.1574+17A>C (ZNF276)	ENSP00000415836.2:n.1574+17A>C
ENST00000561536.5:n.1333+17A>C (ZNF276)
ENST00000561667.2:c.*3472+321T>G (FANCA)	ENSP00000512522.1:n.*3472+321T>G
ENST00000562530.5:c.*474+17A>C (ZNF276)	ENSP00000455466.1:n.*474+17A>C
ENST00000563983.5:n.1562+17A>C (ZNF276)
ENST00000564004.5:n.2250+17A>C (ZNF276)
ENST00000568064.5:c.*13A>C (ZNF276)	ENSP00000457210.1:n.*13A>C
ENST00000568295.5:c.*474+17A>C (ZNF276)	ENSP00000457313.1:n.*474+17A>C
ENST00000568369.6:c.*776T>G (FANCA)	ENSP00000456829.1:n.*776T>G
ENST00000569901.1:n.194+17A>C (ZNF276)
XM_005256324.3:c.1523+17A>C (ZNF276)	XP_005256381.1:n.1523+17A>C
XM_005256328.3:c.932+17A>C (ZNF276)	XP_005256385.1:n.932+17A>C
XM_006721337.1:c.1349+17A>C (ZNF276)	XP_006721400.1:n.1349+17A>C
XM_011523460.1:c.1349+17A>C (ZNF276)	XP_011521762.1:n.1349+17A>C
XM_017023890.1:c.932+17A>C (ZNF276)	XP_016879379.1:n.932+17A>C
XR_001752030.1:n.2793+17A>C (ZNF276)
XR_001752031.1:n.1737+17A>C (ZNF276)
XR_002957853.1:n.2153+17A>C (ZNF276)
XR_243507.2:n.1652+17A>C (ZNF276)
XR_429740.1:n.1756+17A>C (ZNF276)
XR_429740.2:n.1756+17A>C (ZNF276)
XR_933484.2:n.1740+17A>C (ZNF276)