Canonical Allele Identifier: CA397483733

Gene: FANCA ZNF276

Linked Data

• MyVariant Identifiers: chr16:g.89805367G>T (hg19) ; chr16:g.89738959G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738959G>T , CM000678.2:g.89738959G>T	GRCh38
NC_000016.9:g.89805367G>T , CM000678.1:g.89805367G>T	GRCh37
NC_000016.8:g.88332868G>T	NCBI36
NG_011706.1:g.82699C>A , LRG_495:g.82699C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2756C>A (FANCA)	ENSP00000512522.1:n.*2756C>A
ENST00000564475.6:c.4187C>A (FANCA)	ENSP00000454977.2:p.Thr1396Asn
ENST00000567510.2:c.2757C>A (FANCA)	ENSP00000455969.1:n.2757C>A
ENST00000568369.6:c.4187C>A (FANCA)	ENSP00000456829.1:p.Thr1396Asn
ENST00000696274.1:n.4144C>A (FANCA)
ENST00000696275.1:c.*3422C>A (FANCA)	ENSP00000512517.1:n.*3422C>A
ENST00000696286.1:c.*96C>A (FANCA)	ENSP00000512523.1:n.*96C>A
ENST00000696287.1:c.4058C>A (FANCA)	ENSP00000512524.1:p.Thr1353Asn
ENST00000696291.1:c.*3615C>A (FANCA)	ENSP00000512530.1:n.*3615C>A
ENST00000389301.8:c.4183C>A (FANCA) MANE Select	ENSP00000373952.3:p.Leu1395Met
ENST00000443381.7:c.*713G>T (ZNF276) MANE Select	ENSP00000415836.2:n.*713G>T
ENST00000289816.9:c.*713G>T (ZNF276)	ENSP00000289816.5:n.*713G>T
ENST00000389301.7:c.4183C>A (FANCA)	ENSP00000373952.3:p.Leu1395Met
ENST00000561722.5:c.436-33C>A (FANCA)	ENSP00000456608.1:n.436-33C>A
ENST00000562424.1:n.454C>A (FANCA)
ENST00000563983.5:n.2546G>T (ZNF276)
ENST00000564475.5:c.517C>A (FANCA)
ENST00000564870.1:c.384C>A (FANCA)
ENST00000567879.5:c.557C>A (FANCA)	ENSP00000457006.1:p.Thr186Asn
ENST00000568369.5:c.4187C>A (FANCA)	ENSP00000456829.1:p.Thr1396Asn
NM_000135.2:c.4183C>A , LRG_495t1:c.4183C>A (FANCA)	NP_000126.2:p.Leu1395Met
NM_001113525.1:c.*713G>T (ZNF276)	NP_001106997.1:n.*713G>T
NM_001286167.1:c.4187C>A (FANCA)	NP_001273096.1:p.Thr1396Asn
NM_152287.3:c.*713G>T (ZNF276)	NP_689500.2:n.*713G>T
NR_110122.1:n.2730G>T (ZNF276)
NR_110126.1:n.2613G>T (ZNF276)
NR_110128.1:n.2536G>T (ZNF276)
NR_110129.1:n.2625G>T (ZNF276)
XM_005256294.3:c.4187C>A (FANCA)	XP_005256351.1:p.Thr1396Asn
XM_011522945.1:c.4058C>A (FANCA)	XP_011521247.1:p.Thr1353Asn
XM_011522946.1:c.3164C>A (FANCA)	XP_011521248.1:p.Thr1055Asn
XM_011522947.1:c.3164C>A (FANCA)	XP_011521249.1:p.Thr1055Asn
XR_933244.1:n.4150C>A (FANCA)
XR_933245.1:n.4087C>A (FANCA)
NM_000135.3:c.4183C>A (FANCA)	NP_000126.2:p.Leu1395Met
NM_001286167.2:c.4187C>A (FANCA)	NP_001273096.1:p.Thr1396Asn
XM_005256294.4:c.4187C>A (FANCA)	XP_005256351.1:p.Thr1396Asn
XM_011522945.2:c.4058C>A (FANCA)	XP_011521247.1:p.Thr1353Asn
XM_011522946.3:c.3164C>A (FANCA)	XP_011521248.1:p.Thr1055Asn
XM_011522947.2:c.3164C>A (FANCA)	XP_011521249.1:p.Thr1055Asn
XM_017023044.2:c.4054C>A (FANCA)	XP_016878533.1:p.Leu1352Met
XM_017023890.1:c.*713G>T (ZNF276)	XP_016879379.1:n.*713G>T
XM_024450189.1:c.3164C>A (FANCA)	XP_024305957.1:p.Thr1055Asn
XR_933244.2:n.4150C>A (FANCA)
XR_933245.2:n.4087C>A (FANCA)
XR_933484.2:n.2724G>T (ZNF276)
NM_000135.4:c.4183C>A (FANCA) MANE Select	NP_000126.2:p.Leu1395Met
NM_001113525.2:c.*713G>T (ZNF276) MANE Select	NP_001106997.1:n.*713G>T
NM_001286167.3:c.4187C>A (FANCA)	NP_001273096.1:p.Thr1396Asn
NM_152287.4:c.*713G>T (ZNF276)	NP_689500.2:n.*713G>T
NR_110122.2:n.2713G>T (ZNF276)
NR_110126.2:n.2596G>T (ZNF276)
NR_110129.2:n.2630G>T (ZNF276)
NR_110128.2:n.2536G>T (ZNF276)