Canonical Allele Identifier: CA7169169

Gene: FANCM

Linked Data

• ClinVar Variation Id: 1148208
• ClinVar RCV Id: RCV001487976
• dbSNP Id: rs770287146
• ExAC: 14:45636209 C / T
• gnomAD v2: 14-45636209-C-T
• gnomAD v4: 14-45167006-C-T
• MyVariant Identifiers: chr14:g.45636209C>T (hg19) ; chr14:g.45167006C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45167006C>T , CM000676.2:g.45167006C>T	GRCh38
NC_000014.8:g.45636209C>T , CM000676.1:g.45636209C>T	GRCh37
NC_000014.7:g.44705959C>T	NCBI36
NG_007417.1:g.36074C>T , LRG_502:g.36074C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.57C>T	ENSP00000450632.2:p.Asn19=
ENST00000556036.6:c.1845C>T	ENSP00000450596.1:p.Asn615=
ENST00000556250.6:c.1638C>T	ENSP00000452033.2:p.Asn546=
ENST00000696641.1:c.1686C>T	ENSP00000512774.1:p.Asn562=
ENST00000696642.1:c.*656C>T	ENSP00000512775.1:n.*656C>T
ENST00000696646.1:c.*656C>T	ENSP00000512777.1:n.*656C>T
ENST00000696647.1:c.1845C>T	ENSP00000512778.1:p.Asn615=
ENST00000696648.1:c.1845C>T	ENSP00000512779.1:p.Asn615=
ENST00000696649.1:c.1845C>T	ENSP00000512780.1:p.Asn615=
ENST00000696650.1:n.1793C>T
ENST00000696658.1:n.2395C>T
ENST00000696662.1:c.1767C>T	ENSP00000512788.1:p.Asn589=
ENST00000696663.1:c.662C>T
ENST00000696664.1:c.662C>T
ENST00000696675.1:c.1845C>T	ENSP00000512799.1:p.Asn615=
ENST00000696683.1:c.662C>T
ENST00000696684.1:c.662C>T
ENST00000696685.1:c.662C>T
ENST00000267430.10:c.1845C>T MANE Select	ENSP00000267430.5:p.Asn615=
ENST00000267430.9:c.1845C>T	ENSP00000267430.5:p.Asn615=
ENST00000542564.6:c.1767C>T	ENSP00000442493.2:p.Asn589=
ENST00000556036.5:c.1845C>T	ENSP00000450596.1:p.Asn615=
ENST00000556250.5:c.393C>T	ENSP00000452033.1:p.Asn131=
NM_001308133.1:c.1767C>T	NP_001295062.1:p.Asn589=
NM_001308134.1:c.1845C>T	NP_001295063.1:p.Asn615=
NM_020937.2:c.1845C>T , LRG_502t1:c.1845C>T	NP_065988.1:p.Asn615=
NM_020937.3:c.1845C>T	NP_065988.1:p.Asn615=
XM_011537034.1:c.1845C>T	XP_011535336.1:p.Asn615=
XM_011537035.1:c.1767C>T	XP_011535337.1:p.Asn589=
XM_011537036.1:c.1845C>T	XP_011535338.1:p.Asn615=
XM_011537034.2:c.1845C>T	XP_011535336.1:p.Asn615=
XM_011537035.3:c.1767C>T	XP_011535337.1:p.Asn589=
XM_017021523.1:c.1845C>T	XP_016877012.1:p.Asn615=
XM_017021524.2:c.882C>T	XP_016877013.1:p.Asn294=
XM_017021525.2:c.660C>T	XP_016877014.1:p.Asn220=
XM_017021526.2:c.660C>T	XP_016877015.1:p.Asn220=
XM_017021527.1:c.660C>T	XP_016877016.1:p.Asn220=
XR_001750470.1:n.1937C>T
XR_001750471.2:n.1937C>T
XR_001750472.1:n.1937C>T
NM_020937.4:c.1845C>T MANE Select	NP_065988.1:p.Asn615=
NM_001308133.2:c.1767C>T	NP_001295062.1:p.Asn589=
NM_001308134.2:c.1845C>T	NP_001295063.1:p.Asn615=