Canonical Allele Identifier: CA397449827

Gene: FANCA

Linked Data

• gnomAD v4: 16-89773312-C-G
• MyVariant Identifiers: chr16:g.89839720C>G (hg19) ; chr16:g.89773312C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89773312C>G , CM000678.2:g.89773312C>G	GRCh38
NC_000016.9:g.89839720C>G , CM000678.1:g.89839720C>G	GRCh37
NC_000016.8:g.88367221C>G	NCBI36
NG_011706.1:g.48346G>C , LRG_495:g.48346G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*163G>C	ENSP00000512522.1:n.*163G>C
ENST00000564475.6:c.1973G>C	ENSP00000454977.2:p.Gly658Ala
ENST00000567205.2:c.1973G>C	ENSP00000457027.2:p.Gly658Ala
ENST00000567284.7:n.2016G>C
ENST00000567510.2:c.469G>C	ENSP00000455969.1:n.469G>C
ENST00000568369.6:c.1973G>C	ENSP00000456829.1:p.Gly658Ala
ENST00000696274.1:n.1934G>C
ENST00000696275.1:c.*1208G>C	ENSP00000512517.1:n.*1208G>C
ENST00000696276.1:n.2016G>C
ENST00000696286.1:c.1973G>C	ENSP00000512523.1:p.Gly658Ala
ENST00000696287.1:c.1973G>C	ENSP00000512524.1:p.Gly658Ala
ENST00000696291.1:c.*1389G>C	ENSP00000512530.1:n.*1389G>C
ENST00000389301.8:c.1973G>C MANE Select	ENSP00000373952.3:p.Gly658Ala
ENST00000389301.7:c.1973G>C	ENSP00000373952.3:p.Gly658Ala
ENST00000567284.6:n.197G>C
ENST00000568369.5:c.1973G>C	ENSP00000456829.1:p.Gly658Ala
NM_000135.2:c.1973G>C , LRG_495t1:c.1973G>C	NP_000126.2:p.Gly658Ala
NM_001286167.1:c.1973G>C	NP_001273096.1:p.Gly658Ala
XM_005256294.3:c.1973G>C	XP_005256351.1:p.Gly658Ala
XM_011522945.1:c.1973G>C	XP_011521247.1:p.Gly658Ala
XM_011522946.1:c.950G>C	XP_011521248.1:p.Gly317Ala
XM_011522947.1:c.950G>C	XP_011521249.1:p.Gly317Ala
XM_011522948.1:c.1973G>C	XP_011521250.1:p.Gly658Ala
XR_933244.1:n.2016G>C
XR_933245.1:n.2016G>C
XR_933246.1:n.2016G>C
XR_933247.1:n.2016G>C
NM_000135.3:c.1973G>C	NP_000126.2:p.Gly658Ala
NM_001286167.2:c.1973G>C	NP_001273096.1:p.Gly658Ala
XM_005256294.4:c.1973G>C	XP_005256351.1:p.Gly658Ala
XM_011522945.2:c.1973G>C	XP_011521247.1:p.Gly658Ala
XM_011522946.3:c.950G>C	XP_011521248.1:p.Gly317Ala
XM_011522947.2:c.950G>C	XP_011521249.1:p.Gly317Ala
XM_011522948.2:c.1973G>C	XP_011521250.1:p.Gly658Ala
XM_017023044.2:c.1973G>C	XP_016878533.1:p.Gly658Ala
XM_017023045.1:c.1973G>C	XP_016878534.1:p.Gly658Ala
XM_024450189.1:c.950G>C	XP_024305957.1:p.Gly317Ala
XR_001751866.1:n.2016G>C
XR_933244.2:n.2016G>C
XR_933245.2:n.2016G>C
XR_933247.2:n.2016G>C
NM_000135.4:c.1973G>C MANE Select	NP_000126.2:p.Gly658Ala
NM_001286167.3:c.1973G>C	NP_001273096.1:p.Gly658Ala