Canonical Allele Identifier: CA393744753

Gene: FANCI POLG

Linked Data

• MyVariant Identifiers: chr15:g.89858562T>C (hg19) ; chr15:g.89315331T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89315331T>C , CM000677.2:g.89315331T>C	GRCh38
NC_000015.9:g.89858562T>C , CM000677.1:g.89858562T>C	GRCh37
NC_000015.8:g.87659566T>C	NCBI36
NG_008218.1:g.24465A>G
NG_011736.1:g.76369T>C , LRG_500:g.76369T>C
NG_008218.2:g.24465A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696717.1:c.3587T>C (FANCI)	ENSP00000512830.1:p.Ile1196Thr
ENST00000696718.1:c.3329T>C (FANCI)	ENSP00000512831.1:p.Ile1110Thr
ENST00000696719.1:c.3866T>C (FANCI)	ENSP00000512832.1:p.Ile1289Thr
ENST00000696721.1:n.5451T>C (FANCI)
ENST00000310775.12:c.3866T>C (FANCI) MANE Select	ENSP00000310842.8:p.Ile1289Thr
ENST00000635831.1:c.73+1375A>G (POLG)
ENST00000674831.1:c.3998T>C (FANCI)	ENSP00000502474.1:p.Ile1333Thr
ENST00000675352.1:n.3071T>C (FANCI)
ENST00000676003.1:c.3824T>C (FANCI)	ENSP00000502254.1:p.Ile1275Thr
ENST00000676110.1:n.3447T>C (FANCI)
ENST00000300027.12:c.3686T>C (FANCI)	ENSP00000300027.8:p.Ile1229Thr
ENST00000310775.11:c.3866T>C (FANCI)	ENSP00000310842.7:p.Ile1289Thr
ENST00000447611.6:c.*210T>C (FANCI)	ENSP00000413249.2:n.*210T>C
ENST00000561894.1:c.3162T>C (FANCI)
ENST00000566615.1:n.449T>C (FANCI)
ENST00000566895.5:n.3873T>C (FANCI)
NM_001113378.1:c.3866T>C , LRG_500t1:c.3866T>C (FANCI)	NP_001106849.1:p.Ile1289Thr
NM_018193.2:c.3686T>C (FANCI)	NP_060663.2:p.Ile1229Thr
XM_011521756.1:c.3866T>C (FANCI)	XP_011520058.1:p.Ile1289Thr
XM_011521757.1:c.3866T>C (FANCI)	XP_011520059.1:p.Ile1289Thr
XM_011521758.1:c.3866T>C (FANCI)	XP_011520060.1:p.Ile1289Thr
XM_011521759.1:c.3866T>C (FANCI)	XP_011520061.1:p.Ile1289Thr
XM_011521760.1:c.3866T>C (FANCI)	XP_011520062.1:p.Ile1289Thr
XM_011521761.1:c.3866T>C (FANCI)	XP_011520063.1:p.Ile1289Thr
XM_011521762.1:c.3866T>C (FANCI)	XP_011520064.1:p.Ile1289Thr
XM_011521763.1:c.3824T>C (FANCI)	XP_011520065.1:p.Ile1275Thr
XM_011521764.1:c.3686T>C (FANCI)	XP_011520066.1:p.Ile1229Thr
XM_011521765.1:c.3587T>C (FANCI)	XP_011520067.1:p.Ile1196Thr
XM_011521766.1:c.3587T>C (FANCI)	XP_011520068.1:p.Ile1196Thr
XM_011521767.1:c.3587T>C (FANCI)	XP_011520069.1:p.Ile1196Thr
XM_011521769.1:c.3521T>C (FANCI)	XP_011520071.1:p.Ile1174Thr
XM_011521756.2:c.3866T>C (FANCI)	XP_011520058.1:p.Ile1289Thr
XM_011521757.2:c.3866T>C (FANCI)	XP_011520059.1:p.Ile1289Thr
XM_011521764.2:c.3686T>C (FANCI)	XP_011520066.1:p.Ile1229Thr
XM_011521767.2:c.3587T>C (FANCI)	XP_011520069.1:p.Ile1196Thr
NM_001113378.2:c.3866T>C (FANCI) MANE Select	NP_001106849.1:p.Ile1289Thr
NM_001376910.1:c.3587T>C (FANCI)	NP_001363839.1:p.Ile1196Thr
NM_001376911.1:c.3866T>C (FANCI)	NP_001363840.1:p.Ile1289Thr
NM_018193.3:c.3686T>C (FANCI)	NP_060663.2:p.Ile1229Thr