Canonical Allele Identifier: CA619511003

Gene: FANCI POLG

Linked Data

• dbSNP Id: rs1410709967
• gnomAD v2: 15-89858474-T-C
• gnomAD v4: 15-89315243-T-C
• MyVariant Identifiers: chr15:g.89858474T>C (hg19) ; chr15:g.89315243T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89315243T>C , CM000677.2:g.89315243T>C	GRCh38
NC_000015.9:g.89858474T>C , CM000677.1:g.89858474T>C	GRCh37
NC_000015.8:g.87659478T>C	NCBI36
NG_008218.1:g.24553A>G
NG_011736.1:g.76281T>C , LRG_500:g.76281T>C
NG_008218.2:g.24553A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696717.1:c.3538-39T>C (FANCI)	ENSP00000512830.1:n.3538-39T>C
ENST00000696718.1:c.3280-39T>C (FANCI)	ENSP00000512831.1:n.3280-39T>C
ENST00000696719.1:c.3817-39T>C (FANCI)	ENSP00000512832.1:n.3817-39T>C
ENST00000696721.1:n.5402-39T>C (FANCI)
ENST00000310775.12:c.3817-39T>C (FANCI) MANE Select	ENSP00000310842.8:n.3817-39T>C
ENST00000635831.1:c.73+1463A>G (POLG)
ENST00000674831.1:c.3949-39T>C (FANCI)	ENSP00000502474.1:n.3949-39T>C
ENST00000675352.1:n.3022-39T>C (FANCI)
ENST00000676003.1:c.3775-39T>C (FANCI)	ENSP00000502254.1:n.3775-39T>C
ENST00000676110.1:n.3398-39T>C (FANCI)
ENST00000300027.12:c.3637-39T>C (FANCI)	ENSP00000300027.8:n.3637-39T>C
ENST00000310775.11:c.3817-39T>C (FANCI)	ENSP00000310842.7:n.3817-39T>C
ENST00000447611.6:c.*161-39T>C (FANCI)	ENSP00000413249.2:n.*161-39T>C
ENST00000561894.1:c.3113-39T>C (FANCI)
ENST00000566615.1:n.400-39T>C (FANCI)
ENST00000566895.5:n.3824-39T>C (FANCI)
NM_001113378.1:c.3817-39T>C , LRG_500t1:c.3817-39T>C (FANCI)	NP_001106849.1:n.3817-39T>C
NM_018193.2:c.3637-39T>C (FANCI)	NP_060663.2:n.3637-39T>C
XM_011521756.1:c.3817-39T>C (FANCI)	XP_011520058.1:n.3817-39T>C
XM_011521757.1:c.3817-39T>C (FANCI)	XP_011520059.1:n.3817-39T>C
XM_011521758.1:c.3817-39T>C (FANCI)	XP_011520060.1:n.3817-39T>C
XM_011521759.1:c.3817-39T>C (FANCI)	XP_011520061.1:n.3817-39T>C
XM_011521760.1:c.3817-39T>C (FANCI)	XP_011520062.1:n.3817-39T>C
XM_011521761.1:c.3817-39T>C (FANCI)	XP_011520063.1:n.3817-39T>C
XM_011521762.1:c.3817-39T>C (FANCI)	XP_011520064.1:n.3817-39T>C
XM_011521763.1:c.3775-39T>C (FANCI)	XP_011520065.1:n.3775-39T>C
XM_011521764.1:c.3637-39T>C (FANCI)	XP_011520066.1:n.3637-39T>C
XM_011521765.1:c.3538-39T>C (FANCI)	XP_011520067.1:n.3538-39T>C
XM_011521766.1:c.3538-39T>C (FANCI)	XP_011520068.1:n.3538-39T>C
XM_011521767.1:c.3538-39T>C (FANCI)	XP_011520069.1:n.3538-39T>C
XM_011521769.1:c.3472-39T>C (FANCI)	XP_011520071.1:n.3472-39T>C
XM_011521756.2:c.3817-39T>C (FANCI)	XP_011520058.1:n.3817-39T>C
XM_011521757.2:c.3817-39T>C (FANCI)	XP_011520059.1:n.3817-39T>C
XM_011521764.2:c.3637-39T>C (FANCI)	XP_011520066.1:n.3637-39T>C
XM_011521767.2:c.3538-39T>C (FANCI)	XP_011520069.1:n.3538-39T>C
NM_001113378.2:c.3817-39T>C (FANCI) MANE Select	NP_001106849.1:n.3817-39T>C
NM_001376910.1:c.3538-39T>C (FANCI)	NP_001363839.1:n.3538-39T>C
NM_001376911.1:c.3817-39T>C (FANCI)	NP_001363840.1:n.3817-39T>C
NM_018193.3:c.3637-39T>C (FANCI)	NP_060663.2:n.3637-39T>C