Canonical Allele Identifier: CA540881979

Gene: FANCD2 FANCD2OS

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10093330G>C , CM000665.2:g.10093330G>C	GRCh38
NC_000003.11:g.10135014G>C , CM000665.1:g.10135014G>C	GRCh37
NC_000003.10:g.10110014G>C	NCBI36
NG_007311.1:g.71902G>C , LRG_306:g.71902G>C
NG_042053.1:g.19902C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001018115.3:c.3888+7G>C (FANCD2) MANE Select	NP_001018125.1:n.3888+7G>C
ENST00000675286.1:c.3888+7G>C (FANCD2) MANE Select	ENSP00000502379.1:n.3888+7G>C
NM_001018115.1:c.3888+7G>C , LRG_306t1:c.3888+7G>C (FANCD2)	NP_001018125.1:n.3888+7G>C
NM_001018115.2:c.3888+7G>C (FANCD2)	NP_001018125.1:n.3888+7G>C
NM_001319984.1:c.3888+7G>C (FANCD2)	NP_001306913.1:n.3888+7G>C
NM_001319984.2:c.3888+7G>C (FANCD2)	NP_001306913.1:n.3888+7G>C
NM_001374253.1:c.3777+7G>C (FANCD2)	NP_001361182.1:n.3777+7G>C
NM_001374254.1:c.3850-959G>C (FANCD2)	NP_001361183.1:n.3850-959G>C
NM_033084.3:c.3888+7G>C , LRG_306t2:c.3888+7G>C (FANCD2)	NP_149075.2:n.3888+7G>C
NM_033084.4:c.3888+7G>C (FANCD2)	NP_149075.2:n.3888+7G>C
NM_033084.6:c.3888+7G>C (FANCD2)	NP_149075.2:n.3888+7G>C
NM_173472.1:c.*43+10868C>G (FANCD2OS)	NP_775743.1:n.*43+10868C>G
NM_173472.2:c.*43+10868C>G (FANCD2OS)	NP_775743.1:n.*43+10868C>G
ENST00000287647.7:c.3888+7G>C (FANCD2)	ENSP00000287647.3:n.3888+7G>C
ENST00000383807.5:c.3888+7G>C (FANCD2)	ENSP00000373318.1:n.3888+7G>C
ENST00000419585.5:c.3888+7G>C (FANCD2)	ENSP00000398754.1:n.3888+7G>C
ENST00000421731.5:c.2293+7G>C (FANCD2)
ENST00000431315.5:n.95+1536C>G (FANCD2OS)
ENST00000436517.5:n.116+1536C>G (FANCD2OS)
ENST00000470028.1:n.36+7G>C (FANCD2)
ENST00000524279.1:c.*43+10868C>G (FANCD2OS)	ENSP00000429663.1:n.*43+10868C>G
ENST00000676013.1:c.3777+7G>C (FANCD2)	ENSP00000501999.1:n.3777+7G>C
ENST00000681997.1:n.2972+7G>C (FANCD2)
ENST00000683263.1:n.2887+7G>C (FANCD2)
ENST00000683312.1:n.594G>C (FANCD2)
ENST00000683933.1:n.647-959G>C (FANCD2)
XM_005264946.2:c.3888+7G>C (FANCD2)	XP_005265003.1:n.3888+7G>C
XM_005264947.2:c.1893+7G>C (FANCD2)	XP_005265004.1:n.1893+7G>C
XM_006713021.2:c.3888+7G>C (FANCD2)	XP_006713084.1:n.3888+7G>C
XM_006713023.2:c.3850-959G>C (FANCD2)	XP_006713086.1:n.3850-959G>C
XM_006713024.2:c.3771+7G>C (FANCD2)	XP_006713087.1:n.3771+7G>C
XM_011533480.1:c.2739+7G>C (FANCD2)	XP_011531782.1:n.2739+7G>C