Canonical Allele Identifier: CA274537591

Gene: FANCI POLG

Linked Data

• dbSNP Id: rs961039020
• gnomAD v2: 15-89859544-TAG-T
• gnomAD v3: 15-89316313-TAG-T
• gnomAD v4: 15-89316313-TAG-T
• MyVariant Identifiers: chr15:g.89859545_89859546del (hg19) ; chr15:g.89316314_89316315del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89316316_89316317del , CM000677.2:g.89316316_89316317del	GRCh38
NC_000015.9:g.89859547_89859548del , CM000677.1:g.89859547_89859548del	GRCh37
NC_000015.8:g.87660551_87660552del	NCBI36
NG_008218.1:g.23481_23482del
NG_011736.1:g.77354_77355del , LRG_500:g.77354_77355del
NG_008218.2:g.23481_23482del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696717.1:c.3646-81_3646-80del (FANCI)	ENSP00000512830.1:n.3646-81_3646-80del
ENST00000696718.1:c.3388-81_3388-80del (FANCI)	ENSP00000512831.1:n.3388-81_3388-80del
ENST00000696719.1:c.3925-81_3925-80del (FANCI)	ENSP00000512832.1:n.3925-81_3925-80del
ENST00000696721.1:n.5510-81_5510-80del (FANCI)
ENST00000310775.12:c.3925-81_3925-80del (FANCI) MANE Select	ENSP00000310842.8:n.3925-81_3925-80del
ENST00000635831.1:c.73+391_73+392del (POLG)
ENST00000674831.1:c.4057-81_4057-80del (FANCI)	ENSP00000502474.1:n.4057-81_4057-80del
ENST00000675352.1:n.3130-81_3130-80del (FANCI)
ENST00000676003.1:c.3883-81_3883-80del (FANCI)	ENSP00000502254.1:n.3883-81_3883-80del
ENST00000676110.1:n.3506-81_3506-80del (FANCI)
ENST00000268124.9:c.*436_*437del (POLG)	ENSP00000268124.5:n.*436_*437del
ENST00000300027.12:c.3745-81_3745-80del (FANCI)	ENSP00000300027.8:n.3745-81_3745-80del
ENST00000310775.11:c.3925-81_3925-80del (FANCI)	ENSP00000310842.7:n.3925-81_3925-80del
ENST00000447611.6:c.*269-81_*269-80del (FANCI)	ENSP00000413249.2:n.*269-81_*269-80del
ENST00000561894.1:c.3221-81_3221-80del (FANCI)
ENST00000566615.1:n.508-81_508-80del (FANCI)
ENST00000566895.5:n.3932-81_3932-80del (FANCI)
ENST00000631044.2:c.*3580_*3581del (POLG)	ENSP00000486730.1:n.*3580_*3581del
NM_001113378.1:c.3925-81_3925-80del , LRG_500t1:c.3925-81_3925-80del (FANCI)	NP_001106849.1:n.3925-81_3925-80del
NM_001126131.1:c.*436_*437del (POLG)	NP_001119603.1:n.*436_*437del
NM_002693.2:c.*436_*437del (POLG)	NP_002684.1:n.*436_*437del
NM_018193.2:c.3745-81_3745-80del (FANCI)	NP_060663.2:n.3745-81_3745-80del
XM_011521756.1:c.3925-81_3925-80del (FANCI)	XP_011520058.1:n.3925-81_3925-80del
XM_011521757.1:c.3925-81_3925-80del (FANCI)	XP_011520059.1:n.3925-81_3925-80del
XM_011521758.1:c.3925-81_3925-80del (FANCI)	XP_011520060.1:n.3925-81_3925-80del
XM_011521759.1:c.3925-81_3925-80del (FANCI)	XP_011520061.1:n.3925-81_3925-80del
XM_011521760.1:c.3925-81_3925-80del (FANCI)	XP_011520062.1:n.3925-81_3925-80del
XM_011521761.1:c.3925-81_3925-80del (FANCI)	XP_011520063.1:n.3925-81_3925-80del
XM_011521762.1:c.3925-81_3925-80del (FANCI)	XP_011520064.1:n.3925-81_3925-80del
XM_011521763.1:c.3883-81_3883-80del (FANCI)	XP_011520065.1:n.3883-81_3883-80del
XM_011521764.1:c.3745-81_3745-80del (FANCI)	XP_011520066.1:n.3745-81_3745-80del
XM_011521765.1:c.3646-81_3646-80del (FANCI)	XP_011520067.1:n.3646-81_3646-80del
XM_011521766.1:c.3646-81_3646-80del (FANCI)	XP_011520068.1:n.3646-81_3646-80del
XM_011521767.1:c.3646-81_3646-80del (FANCI)	XP_011520069.1:n.3646-81_3646-80del
XM_011521769.1:c.3580-81_3580-80del (FANCI)	XP_011520071.1:n.3580-81_3580-80del
XM_011521756.2:c.3925-81_3925-80del (FANCI)	XP_011520058.1:n.3925-81_3925-80del
XM_011521757.2:c.3925-81_3925-80del (FANCI)	XP_011520059.1:n.3925-81_3925-80del
XM_011521764.2:c.3745-81_3745-80del (FANCI)	XP_011520066.1:n.3745-81_3745-80del
XM_011521767.2:c.3646-81_3646-80del (FANCI)	XP_011520069.1:n.3646-81_3646-80del
NM_001113378.2:c.3925-81_3925-80del (FANCI) MANE Select	NP_001106849.1:n.3925-81_3925-80del
NM_001376910.1:c.3646-81_3646-80del (FANCI)	NP_001363839.1:n.3646-81_3646-80del
NM_001376911.1:c.3925-81_3925-80del (FANCI)	NP_001363840.1:n.3925-81_3925-80del
NM_018193.3:c.3745-81_3745-80del (FANCI)	NP_060663.2:n.3745-81_3745-80del