Canonical Allele Identifier: CA2575828188

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89316310A>C , CM000677.2:g.89316310A>C GRCh38
NC_000015.9:g.89859541A>C , CM000677.1:g.89859541A>C GRCh37
NC_000015.8:g.87660545A>C NCBI36
NG_008218.1:g.23486T>G
NG_011736.1:g.77348A>C , LRG_500:g.77348A>C
NG_008218.2:g.23486T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696717.1:c.3646-87A>C (FANCI) ENSP00000512830.1:n.3646-87A>C
ENST00000696718.1:c.3388-87A>C (FANCI) ENSP00000512831.1:n.3388-87A>C
ENST00000696719.1:c.3925-87A>C (FANCI) ENSP00000512832.1:n.3925-87A>C
ENST00000696721.1:n.5510-87A>C (FANCI)
ENST00000310775.12:c.3925-87A>C (FANCI) MANE Select ENSP00000310842.8:n.3925-87A>C
ENST00000635831.1:c.73+396T>G (POLG)
ENST00000674831.1:c.4057-87A>C (FANCI) ENSP00000502474.1:n.4057-87A>C
ENST00000675352.1:n.3130-87A>C (FANCI)
ENST00000676003.1:c.3883-87A>C (FANCI) ENSP00000502254.1:n.3883-87A>C
ENST00000676110.1:n.3506-87A>C (FANCI)
ENST00000268124.9:c.*441T>G (POLG) ENSP00000268124.5:n.*441T>G
ENST00000300027.12:c.3745-87A>C (FANCI) ENSP00000300027.8:n.3745-87A>C
ENST00000310775.11:c.3925-87A>C (FANCI) ENSP00000310842.7:n.3925-87A>C
ENST00000447611.6:c.*269-87A>C (FANCI) ENSP00000413249.2:n.*269-87A>C
ENST00000561894.1:c.3221-87A>C (FANCI)
ENST00000566615.1:n.508-87A>C (FANCI)
ENST00000566895.5:n.3932-87A>C (FANCI)
ENST00000631044.2:c.*3585T>G (POLG) ENSP00000486730.1:n.*3585T>G
NM_001113378.1:c.3925-87A>C , LRG_500t1:c.3925-87A>C (FANCI) NP_001106849.1:n.3925-87A>C
NM_001126131.1:c.*441T>G (POLG) NP_001119603.1:n.*441T>G
NM_002693.2:c.*441T>G (POLG) NP_002684.1:n.*441T>G
NM_018193.2:c.3745-87A>C (FANCI) NP_060663.2:n.3745-87A>C
XM_011521756.1:c.3925-87A>C (FANCI) XP_011520058.1:n.3925-87A>C
XM_011521757.1:c.3925-87A>C (FANCI) XP_011520059.1:n.3925-87A>C
XM_011521758.1:c.3925-87A>C (FANCI) XP_011520060.1:n.3925-87A>C
XM_011521759.1:c.3925-87A>C (FANCI) XP_011520061.1:n.3925-87A>C
XM_011521760.1:c.3925-87A>C (FANCI) XP_011520062.1:n.3925-87A>C
XM_011521761.1:c.3925-87A>C (FANCI) XP_011520063.1:n.3925-87A>C
XM_011521762.1:c.3925-87A>C (FANCI) XP_011520064.1:n.3925-87A>C
XM_011521763.1:c.3883-87A>C (FANCI) XP_011520065.1:n.3883-87A>C
XM_011521764.1:c.3745-87A>C (FANCI) XP_011520066.1:n.3745-87A>C
XM_011521765.1:c.3646-87A>C (FANCI) XP_011520067.1:n.3646-87A>C
XM_011521766.1:c.3646-87A>C (FANCI) XP_011520068.1:n.3646-87A>C
XM_011521767.1:c.3646-87A>C (FANCI) XP_011520069.1:n.3646-87A>C
XM_011521769.1:c.3580-87A>C (FANCI) XP_011520071.1:n.3580-87A>C
XM_011521756.2:c.3925-87A>C (FANCI) XP_011520058.1:n.3925-87A>C
XM_011521757.2:c.3925-87A>C (FANCI) XP_011520059.1:n.3925-87A>C
XM_011521764.2:c.3745-87A>C (FANCI) XP_011520066.1:n.3745-87A>C
XM_011521767.2:c.3646-87A>C (FANCI) XP_011520069.1:n.3646-87A>C
NM_001113378.2:c.3925-87A>C (FANCI) MANE Select NP_001106849.1:n.3925-87A>C
NM_001376910.1:c.3646-87A>C (FANCI) NP_001363839.1:n.3646-87A>C
NM_001376911.1:c.3925-87A>C (FANCI) NP_001363840.1:n.3925-87A>C
NM_018193.3:c.3745-87A>C (FANCI) NP_060663.2:n.3745-87A>C