Canonical Allele Identifier: CA2250653

Gene: FANCD2 FANCD2OS

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10098740A>G , CM000665.2:g.10098740A>G	GRCh38
NC_000003.11:g.10140424A>G , CM000665.1:g.10140424A>G	GRCh37
NC_000003.10:g.10115424A>G	NCBI36
NG_007311.1:g.77312A>G , LRG_306:g.77312A>G
NG_042053.1:g.14492T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681997.1:n.3290A>G (FANCD2)
ENST00000683263.1:n.3205A>G (FANCD2)
ENST00000683312.1:n.3757A>G (FANCD2)
ENST00000675286.1:c.4206A>G (FANCD2) MANE Select	ENSP00000502379.1:p.Gln1402=
ENST00000676013.1:c.4095A>G (FANCD2)	ENSP00000501999.1:p.Gln1365=
ENST00000287647.7:c.4206A>G (FANCD2)	ENSP00000287647.3:p.Gln1402=
ENST00000383807.5:c.4206A>G (FANCD2)	ENSP00000373318.1:p.Gln1402=
ENST00000419585.5:c.4206A>G (FANCD2)	ENSP00000398754.1:p.Gln1402=
ENST00000421731.5:c.2611A>G (FANCD2)
ENST00000431315.5:n.71-3850T>C (FANCD2OS)
ENST00000470028.1:n.279A>G (FANCD2)
ENST00000524279.1:c.*43+5458T>C (FANCD2OS)	ENSP00000429663.1:n.*43+5458T>C
NM_001018115.1:c.4206A>G , LRG_306t1:c.4206A>G (FANCD2)	NP_001018125.1:p.Gln1402=
NM_033084.3:c.4206A>G , LRG_306t2:c.4206A>G (FANCD2)	NP_149075.2:p.Gln1402=
NM_173472.1:c.*43+5458T>C (FANCD2OS)	NP_775743.1:n.*43+5458T>C
XM_005264946.2:c.4206A>G (FANCD2)	XP_005265003.1:p.Gln1402=
XM_005264947.2:c.2211A>G (FANCD2)	XP_005265004.1:p.Gln737=
XM_006713021.2:c.4206A>G (FANCD2)	XP_006713084.1:p.Gln1402=
XM_006713023.2:c.4167A>G (FANCD2)	XP_006713086.1:p.Gln1389=
XM_006713024.2:c.4089A>G (FANCD2)	XP_006713087.1:p.Gln1363=
XM_011533480.1:c.3057A>G (FANCD2)	XP_011531782.1:p.Gln1019=
NM_001018115.2:c.4206A>G (FANCD2)	NP_001018125.1:p.Gln1402=
NM_001319984.1:c.4206A>G (FANCD2)	NP_001306913.1:p.Gln1402=
NM_033084.4:c.4206A>G (FANCD2)	NP_149075.2:p.Gln1402=
NM_001018115.3:c.4206A>G (FANCD2) MANE Select	NP_001018125.1:p.Gln1402=
NM_001319984.2:c.4206A>G (FANCD2)	NP_001306913.1:p.Gln1402=
NM_001374253.1:c.4095A>G (FANCD2)	NP_001361182.1:p.Gln1365=
NM_001374254.1:c.4167A>G (FANCD2)	NP_001361183.1:p.Gln1389=
NM_033084.6:c.4206A>G (FANCD2)	NP_149075.2:p.Gln1402=
NM_173472.2:c.*43+5458T>C (FANCD2OS)	NP_775743.1:n.*43+5458T>C