Canonical Allele Identifier: CA1139664981

Gene: FANCA

Linked Data

• ClinVar Variation Id: 974075
• ClinVar RCV Id: RCV001256315

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89809030_89816657del , CM000678.2:g.89809030_89816657del	GRCh38
NC_000016.9:g.89875438_89883065del , CM000678.1:g.89875438_89883065del	GRCh37
NC_000016.8:g.88402939_88410566del	NCBI36
NG_011706.1:g.5001_12628del , LRG_495:g.5001_12628del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000564475.6:c.-42_523-663del
ENST00000567205.2:c.-42_523-663del
ENST00000567284.7:n.2_566-663del
ENST00000567621.6:c.-42_523-663del
ENST00000568369.6:c.-42_523-663del
ENST00000696275.1:c.-42_523-663del
ENST00000696276.1:n.2_566-663del
ENST00000696277.1:c.-42_523-663del
ENST00000696287.1:c.-42_523-663del
ENST00000696291.1:c.-42_522+1677del
ENST00000389302.7:c.-42_523-663del
ENST00000543736.5:c.-42_427-663del
NM_000135.2:c.-42_523-663del , LRG_495t1:c.-42_523-663del
NM_001018112.1:c.-42_523-663del
NM_001286167.1:c.-42_523-663del
XM_005256294.3:c.-42_523-663del
XM_011522945.1:c.-42_523-663del
XM_011522948.1:c.-42_523-663del
XR_933244.1:n.2_566-663del
XR_933245.1:n.2_566-663del
XR_933246.1:n.2_566-663del
XR_933247.1:n.2_566-663del
NM_000135.3:c.-42_523-663del
NM_001018112.2:c.-42_523-663del
NM_001286167.2:c.-42_523-663del
NM_001351830.1:c.-42_427-663del
XM_005256294.4:c.-42_523-663del
XM_011522945.2:c.-42_523-663del
XM_011522948.2:c.-42_523-663del
XM_017023044.2:c.-42_523-663del
XM_017023045.1:c.-42_523-663del
XM_017023046.1:c.-42_523-663del
XR_001751866.1:n.2_566-663del
XR_001751867.1:n.2_566-663del
XR_001751868.2:n.2_566-663del
XR_002957793.1:n.2_566-663del
XR_933244.2:n.2_566-663del
XR_933245.2:n.2_566-663del
XR_933247.2:n.2_566-663del