Canonical Allele Identifier: CA2250568

Gene: FANCD2 FANCD2OS

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10094322C>T , CM000665.2:g.10094322C>T	GRCh38
NC_000003.11:g.10136006C>T , CM000665.1:g.10136006C>T	GRCh37
NC_000003.10:g.10111006C>T	NCBI36
NG_007311.1:g.72894C>T , LRG_306:g.72894C>T
NG_042053.1:g.18910G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001018115.3:c.3922C>T (FANCD2) MANE Select	NP_001018125.1:p.Gln1308Ter
ENST00000675286.1:c.3922C>T (FANCD2) MANE Select	ENSP00000502379.1:p.Gln1308Ter
NM_001018115.1:c.3922C>T , LRG_306t1:c.3922C>T (FANCD2)	NP_001018125.1:p.Gln1308Ter
NM_001018115.2:c.3922C>T (FANCD2)	NP_001018125.1:p.Gln1308Ter
NM_001319984.1:c.3922C>T (FANCD2)	NP_001306913.1:p.Gln1308Ter
NM_001319984.2:c.3922C>T (FANCD2)	NP_001306913.1:p.Gln1308Ter
NM_001374253.1:c.3811C>T (FANCD2)	NP_001361182.1:p.Gln1271Ter
NM_001374254.1:c.3883C>T (FANCD2)	NP_001361183.1:p.Gln1295Ter
NM_033084.3:c.3922C>T , LRG_306t2:c.3922C>T (FANCD2)	NP_149075.2:p.Gln1308Ter
NM_033084.4:c.3922C>T (FANCD2)	NP_149075.2:p.Gln1308Ter
NM_033084.6:c.3922C>T (FANCD2)	NP_149075.2:p.Gln1308Ter
NM_173472.1:c.*43+9876G>A (FANCD2OS)	NP_775743.1:n.*43+9876G>A
NM_173472.2:c.*43+9876G>A (FANCD2OS)	NP_775743.1:n.*43+9876G>A
ENST00000287647.7:c.3922C>T (FANCD2)	ENSP00000287647.3:p.Gln1308Ter
ENST00000383807.5:c.3922C>T (FANCD2)	ENSP00000373318.1:p.Gln1308Ter
ENST00000419585.5:c.3922C>T (FANCD2)	ENSP00000398754.1:p.Gln1308Ter
ENST00000421731.5:c.2327C>T (FANCD2)
ENST00000431315.5:n.95+544G>A (FANCD2OS)
ENST00000436517.5:n.116+544G>A (FANCD2OS)
ENST00000470028.1:n.37-878C>T (FANCD2)
ENST00000524279.1:c.*43+9876G>A (FANCD2OS)	ENSP00000429663.1:n.*43+9876G>A
ENST00000676013.1:c.3811C>T (FANCD2)	ENSP00000501999.1:p.Gln1271Ter
ENST00000681997.1:n.3006C>T (FANCD2)
ENST00000683263.1:n.2921C>T (FANCD2)
ENST00000683312.1:n.1586C>T (FANCD2)
ENST00000683933.1:n.680C>T (FANCD2)
XM_005264946.2:c.3922C>T (FANCD2)	XP_005265003.1:p.Gln1308Ter
XM_005264947.2:c.1927C>T (FANCD2)	XP_005265004.1:p.Gln643Ter
XM_006713021.2:c.3922C>T (FANCD2)	XP_006713084.1:p.Gln1308Ter
XM_006713023.2:c.3883C>T (FANCD2)	XP_006713086.1:p.Gln1295Ter
XM_006713024.2:c.3805C>T (FANCD2)	XP_006713087.1:p.Gln1269Ter
XM_011533480.1:c.2773C>T (FANCD2)	XP_011531782.1:p.Gln925Ter