Canonical Allele Identifier: CA286568058

Gene: FANCA

Linked Data

• dbSNP Id: rs35697781
• MyVariant Identifiers: chr16:g.89839621_89839622insT (hg19) ; chr16:g.89773213_89773214insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89773213_89773214insT , CM000678.2:g.89773213_89773214insT	GRCh38
NC_000016.9:g.89839621_89839622insT , CM000678.1:g.89839621_89839622insT	GRCh37
NC_000016.8:g.88367122_88367123insT	NCBI36
NG_011706.1:g.48444_48445insA , LRG_495:g.48444_48445insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000561667.2:c.*204+57_*204+58insA	ENSP00000512522.1:n.*204+57_*204+58insA
ENST00000564475.6:c.2014+57_2014+58insA	ENSP00000454977.2:n.2014+57_2014+58insA
ENST00000567205.2:c.2014+57_2014+58insA	ENSP00000457027.2:n.2014+57_2014+58insA
ENST00000567284.7:n.2057+57_2057+58insA
ENST00000567510.2:c.510+57_510+58insA	ENSP00000455969.1:n.510+57_510+58insA
ENST00000568369.6:c.2014+57_2014+58insA	ENSP00000456829.1:n.2014+57_2014+58insA
ENST00000696274.1:n.1975+57_1975+58insA
ENST00000696275.1:c.*1249+57_*1249+58insA	ENSP00000512517.1:n.*1249+57_*1249+58insA...
ENST00000696276.1:n.2057+57_2057+58insA
ENST00000696286.1:c.2014+57_2014+58insA	ENSP00000512523.1:n.2014+57_2014+58insA
ENST00000696287.1:c.2014+57_2014+58insA	ENSP00000512524.1:n.2014+57_2014+58insA
ENST00000696291.1:c.*1430+57_*1430+58insA	ENSP00000512530.1:n.*1430+57_*1430+58insA...
ENST00000389301.8:c.2014+57_2014+58insA MANE Select	ENSP00000373952.3:n.2014+57_2014+58insA
ENST00000389301.7:c.2014+57_2014+58insA	ENSP00000373952.3:n.2014+57_2014+58insA
ENST00000567284.6:n.238+57_238+58insA
ENST00000568369.5:c.2014+57_2014+58insA	ENSP00000456829.1:n.2014+57_2014+58insA
NM_000135.2:c.2014+57_2014+58insA , LRG_495t1:c.2014+57_2014+58insA	NP_000126.2:n.2014+57_2014+58insA
NM_001286167.1:c.2014+57_2014+58insA	NP_001273096.1:n.2014+57_2014+58insA
XM_005256294.3:c.2014+57_2014+58insA	XP_005256351.1:n.2014+57_2014+58insA
XM_011522945.1:c.2014+57_2014+58insA	XP_011521247.1:n.2014+57_2014+58insA
XM_011522946.1:c.991+57_991+58insA	XP_011521248.1:n.991+57_991+58insA
XM_011522947.1:c.991+57_991+58insA	XP_011521249.1:n.991+57_991+58insA
XM_011522948.1:c.2014+57_2014+58insA	XP_011521250.1:n.2014+57_2014+58insA
XR_933244.1:n.2057+57_2057+58insA
XR_933245.1:n.2057+57_2057+58insA
XR_933246.1:n.2057+57_2057+58insA
XR_933247.1:n.2057+57_2057+58insA
NM_000135.3:c.2014+57_2014+58insA	NP_000126.2:n.2014+57_2014+58insA
NM_001286167.2:c.2014+57_2014+58insA	NP_001273096.1:n.2014+57_2014+58insA
XM_005256294.4:c.2014+57_2014+58insA	XP_005256351.1:n.2014+57_2014+58insA
XM_011522945.2:c.2014+57_2014+58insA	XP_011521247.1:n.2014+57_2014+58insA
XM_011522946.3:c.991+57_991+58insA	XP_011521248.1:n.991+57_991+58insA
XM_011522947.2:c.991+57_991+58insA	XP_011521249.1:n.991+57_991+58insA
XM_011522948.2:c.2014+57_2014+58insA	XP_011521250.1:n.2014+57_2014+58insA
XM_017023044.2:c.2014+57_2014+58insA	XP_016878533.1:n.2014+57_2014+58insA
XM_017023045.1:c.2014+57_2014+58insA	XP_016878534.1:n.2014+57_2014+58insA
XM_024450189.1:c.991+57_991+58insA	XP_024305957.1:n.991+57_991+58insA
XR_001751866.1:n.2057+57_2057+58insA
XR_933244.2:n.2057+57_2057+58insA
XR_933245.2:n.2057+57_2057+58insA
XR_933247.2:n.2057+57_2057+58insA
NM_000135.4:c.2014+57_2014+58insA MANE Select	NP_000126.2:n.2014+57_2014+58insA
NM_001286167.3:c.2014+57_2014+58insA	NP_001273096.1:n.2014+57_2014+58insA