Canonical Allele Identifier: CA1345049609

Gene: FANCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10064709A= , CM000665.2:g.10064709A=	GRCh38
NC_000003.11:g.10106393A= , CM000665.1:g.10106393A=	GRCh37
NC_000003.10:g.10081393A=	NCBI36
NG_007311.1:g.43281A= , LRG_306:g.43281A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681997.1:n.1106-20A=
ENST00000683263.1:n.1021-20A=
ENST00000675286.1:c.2022-20A= MANE Select	ENSP00000502379.1:n.2022-20A=
ENST00000676013.1:c.1911-20A=	ENSP00000501999.1:n.1911-20A=
ENST00000287647.7:c.2022-20A=	ENSP00000287647.3:n.2022-20A=
ENST00000383807.5:c.2022-20A=	ENSP00000373318.1:n.2022-20A=
ENST00000419585.5:c.2022-20A=	ENSP00000398754.1:n.2022-20A=
ENST00000421731.5:c.521-20A=
ENST00000470757.5:n.76-20A=
ENST00000480909.1:n.17A=
NM_001018115.1:c.2022-20A= , LRG_306t1:c.2022-20A=	NP_001018125.1:n.2022-20A=
NM_033084.3:c.2022-20A= , LRG_306t2:c.2022-20A=	NP_149075.2:n.2022-20A=
XM_005264946.2:c.2022-20A=	XP_005265003.1:n.2022-20A=
XM_005264947.2:c.27-20A=	XP_005265004.1:n.27-20A=
XM_006713021.2:c.2022-20A=	XP_006713084.1:n.2022-20A=
XM_006713023.2:c.2022-20A=	XP_006713086.1:n.2022-20A=
XM_006713024.2:c.2022-20A=	XP_006713087.1:n.2022-20A=
XM_011533479.1:c.2022-20A=	XP_011531781.1:n.2022-20A=
XM_011533480.1:c.873-20A=	XP_011531782.1:n.873-20A=
XR_940391.1:n.2142-20A=
NM_001018115.2:c.2022-20A=	NP_001018125.1:n.2022-20A=
NM_001319984.1:c.2022-20A=	NP_001306913.1:n.2022-20A=
NM_033084.4:c.2022-20A=	NP_149075.2:n.2022-20A=
NM_001018115.3:c.2022-20A= MANE Select	NP_001018125.1:n.2022-20A=
NM_001319984.2:c.2022-20A=	NP_001306913.1:n.2022-20A=
NM_001374253.1:c.1911-20A=	NP_001361182.1:n.1911-20A=
NM_001374254.1:c.2022-20A=	NP_001361183.1:n.2022-20A=
NM_033084.6:c.2022-20A=	NP_149075.2:n.2022-20A=