Canonical Allele Identifier: CA397437831

Gene: FANCA

Linked Data

• MyVariant Identifiers: chr16:g.89831302A>T (hg19) ; chr16:g.89764894A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89764894A>T , CM000678.2:g.89764894A>T	GRCh38
NC_000016.9:g.89831302A>T , CM000678.1:g.89831302A>T	GRCh37
NC_000016.8:g.88358803A>T	NCBI36
NG_011706.1:g.56764T>A , LRG_495:g.56764T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*1268T>A	ENSP00000512522.1:n.*1268T>A
ENST00000564475.6:c.2774T>A	ENSP00000454977.2:p.Val925Asp
ENST00000567510.2:c.1473T>A	ENSP00000455969.1:n.1473T>A
ENST00000568369.6:c.2774T>A	ENSP00000456829.1:p.Val925Asp
ENST00000696274.1:n.2735T>A
ENST00000696275.1:c.*2009T>A	ENSP00000512517.1:n.*2009T>A
ENST00000696276.1:n.2817T>A
ENST00000696286.1:c.2774T>A	ENSP00000512523.1:p.Val925Asp
ENST00000696287.1:c.2774T>A	ENSP00000512524.1:p.Val925Asp
ENST00000696291.1:c.*2494T>A	ENSP00000512530.1:n.*2494T>A
ENST00000389301.8:c.2774T>A MANE Select	ENSP00000373952.3:p.Val925Asp
ENST00000305699.15:n.146T>A
ENST00000389301.7:c.2774T>A	ENSP00000373952.3:p.Val925Asp
ENST00000561660.1:c.151T>A
ENST00000563318.1:c.180T>A
ENST00000563510.5:c.54T>A
ENST00000567988.5:c.111T>A
ENST00000568369.5:c.2774T>A	ENSP00000456829.1:p.Val925Asp
NM_000135.2:c.2774T>A , LRG_495t1:c.2774T>A	NP_000126.2:p.Val925Asp
NM_001286167.1:c.2774T>A	NP_001273096.1:p.Val925Asp
XM_005256294.3:c.2774T>A	XP_005256351.1:p.Val925Asp
XM_011522945.1:c.2774T>A	XP_011521247.1:p.Val925Asp
XM_011522946.1:c.1751T>A	XP_011521248.1:p.Val584Asp
XM_011522947.1:c.1751T>A	XP_011521249.1:p.Val584Asp
XR_933244.1:n.2817T>A
XR_933245.1:n.2817T>A
XR_933246.1:n.2817T>A
NM_000135.3:c.2774T>A	NP_000126.2:p.Val925Asp
NM_001286167.2:c.2774T>A	NP_001273096.1:p.Val925Asp
XM_005256294.4:c.2774T>A	XP_005256351.1:p.Val925Asp
XM_011522945.2:c.2774T>A	XP_011521247.1:p.Val925Asp
XM_011522946.3:c.1751T>A	XP_011521248.1:p.Val584Asp
XM_011522947.2:c.1751T>A	XP_011521249.1:p.Val584Asp
XM_017023044.2:c.2774T>A	XP_016878533.1:p.Val925Asp
XM_017023045.1:c.2774T>A	XP_016878534.1:p.Val925Asp
XM_024450189.1:c.1751T>A	XP_024305957.1:p.Val584Asp
XR_001751866.1:n.2817T>A
XR_933244.2:n.2817T>A
XR_933245.2:n.2817T>A
XR_933247.2:n.2946T>A
NM_000135.4:c.2774T>A MANE Select	NP_000126.2:p.Val925Asp
NM_001286167.3:c.2774T>A	NP_001273096.1:p.Val925Asp