Canonical Allele Identifier: CA397438064

Gene: FANCA

Linked Data

• MyVariant Identifiers: chr16:g.89831332G>T (hg19) ; chr16:g.89764924G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89764924G>T , CM000678.2:g.89764924G>T	GRCh38
NC_000016.9:g.89831332G>T , CM000678.1:g.89831332G>T	GRCh37
NC_000016.8:g.88358833G>T	NCBI36
NG_011706.1:g.56734C>A , LRG_495:g.56734C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*1238C>A	ENSP00000512522.1:n.*1238C>A
ENST00000564475.6:c.2744C>A	ENSP00000454977.2:p.Thr915Asn
ENST00000567510.2:c.1443C>A	ENSP00000455969.1:n.1443C>A
ENST00000568369.6:c.2744C>A	ENSP00000456829.1:p.Thr915Asn
ENST00000696274.1:n.2705C>A
ENST00000696275.1:c.*1979C>A	ENSP00000512517.1:n.*1979C>A
ENST00000696276.1:n.2787C>A
ENST00000696286.1:c.2744C>A	ENSP00000512523.1:p.Thr915Asn
ENST00000696287.1:c.2744C>A	ENSP00000512524.1:p.Thr915Asn
ENST00000696291.1:c.*2464C>A	ENSP00000512530.1:n.*2464C>A
ENST00000389301.8:c.2744C>A MANE Select	ENSP00000373952.3:p.Thr915Asn
ENST00000305699.15:n.116C>A
ENST00000389301.7:c.2744C>A	ENSP00000373952.3:p.Thr915Asn
ENST00000561660.1:c.121C>A
ENST00000563318.1:c.150C>A
ENST00000563510.5:c.24C>A
ENST00000567988.5:c.81C>A
ENST00000568369.5:c.2744C>A	ENSP00000456829.1:p.Thr915Asn
NM_000135.2:c.2744C>A , LRG_495t1:c.2744C>A	NP_000126.2:p.Thr915Asn
NM_001286167.1:c.2744C>A	NP_001273096.1:p.Thr915Asn
XM_005256294.3:c.2744C>A	XP_005256351.1:p.Thr915Asn
XM_011522945.1:c.2744C>A	XP_011521247.1:p.Thr915Asn
XM_011522946.1:c.1721C>A	XP_011521248.1:p.Thr574Asn
XM_011522947.1:c.1721C>A	XP_011521249.1:p.Thr574Asn
XR_933244.1:n.2787C>A
XR_933245.1:n.2787C>A
XR_933246.1:n.2787C>A
NM_000135.3:c.2744C>A	NP_000126.2:p.Thr915Asn
NM_001286167.2:c.2744C>A	NP_001273096.1:p.Thr915Asn
XM_005256294.4:c.2744C>A	XP_005256351.1:p.Thr915Asn
XM_011522945.2:c.2744C>A	XP_011521247.1:p.Thr915Asn
XM_011522946.3:c.1721C>A	XP_011521248.1:p.Thr574Asn
XM_011522947.2:c.1721C>A	XP_011521249.1:p.Thr574Asn
XM_017023044.2:c.2744C>A	XP_016878533.1:p.Thr915Asn
XM_017023045.1:c.2744C>A	XP_016878534.1:p.Thr915Asn
XM_024450189.1:c.1721C>A	XP_024305957.1:p.Thr574Asn
XR_001751866.1:n.2787C>A
XR_933244.2:n.2787C>A
XR_933245.2:n.2787C>A
XR_933247.2:n.2916C>A
NM_000135.4:c.2744C>A MANE Select	NP_000126.2:p.Thr915Asn
NM_001286167.3:c.2744C>A	NP_001273096.1:p.Thr915Asn