Canonical Allele Identifier: CA2785168576

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95172160_95172161insCACACCCAAC , CM000671.2:g.95172160_95172161insCACACCCAAC	GRCh38
NC_000009.11:g.97934442_97934443insCACACCCAAC , CM000671.1:g.97934442_97934443insCACACCCAAC	GRCh37
NC_000009.10:g.96974263_96974264insCACACCCAAC	NCBI36
NG_011707.1:g.150549_150550insGTTGGGTGTG , LRG_497:g.150549_150550insGTTGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.737-14_737-13insGTTGGGTGTG
ENST00000289081.8:c.346-14_346-13insGTTGGGTGTG MANE Select	ENSP00000289081.3:n.346-14_346-13insGTTGGGTGTG
ENST00000375305.6:c.346-14_346-13insGTTGGGTGTG	ENSP00000364454.1:n.346-14_346-13insGTTGGGTGTG
ENST00000490972.7:c.346-14_346-13insGTTGGGTGTG	ENSP00000479931.1:n.346-14_346-13insGTTGGGTGTG
ENST00000636777.1:n.404-14_404-13insGTTGGGTGTG
ENST00000647778.1:c.346-14_346-13insGTTGGGTGTG	ENSP00000498125.1:n.346-14_346-13insGTTGGGTGTG
ENST00000647882.1:c.346-14_346-13insGTTGGGTGTG	ENSP00000497025.1:n.346-14_346-13insGTTGGGTGTG
ENST00000649334.1:c.491-14_491-13insGTTGGGTGTG	ENSP00000497735.1:n.491-14_491-13insGTTGGGTGTG
ENST00000649701.1:n.61-14_61-13insGTTGGGTGTG
ENST00000289081.7:c.346-14_346-13insGTTGGGTGTG	ENSP00000289081.3:n.346-14_346-13insGTTGGGTGTG
ENST00000375305.5:c.346-14_346-13insGTTGGGTGTG	ENSP00000364454.1:n.346-14_346-13insGTTGGGTGTG
ENST00000433829.1:c.346-14_346-13insGTTGGGTGTG	ENSP00000406908.1:n.346-14_346-13insGTTGGGTGTG
ENST00000474949.1:n.703-14_703-13insGTTGGGTGTG
ENST00000490972.6:c.346-14_346-13insGTTGGGTGTG	ENSP00000479931.1:n.346-14_346-13insGTTGGGTGTG
NM_000136.2:c.346-14_346-13insGTTGGGTGTG , LRG_497t1:c.346-14_346-13insGTTGGGTGTG	NP_000127.2:n.346-14_346-13insGTTGGGTGTG
NM_001243743.1:c.346-14_346-13insGTTGGGTGTG	NP_001230672.1:n.346-14_346-13insGTTGGGTGTG
NM_001243744.1:c.346-14_346-13insGTTGGGTGTG	NP_001230673.1:n.346-14_346-13insGTTGGGTGTG
XM_006717001.1:c.346-14_346-13insGTTGGGTGTG	XP_006717064.1:n.346-14_346-13insGTTGGGTGTG
XM_006717002.2:c.346-14_346-13insGTTGGGTGTG	XP_006717065.1:n.346-14_346-13insGTTGGGTGTG
XM_006717004.2:c.346-14_346-13insGTTGGGTGTG	XP_006717067.1:n.346-14_346-13insGTTGGGTGTG
XM_011518365.1:c.346-14_346-13insGTTGGGTGTG	XP_011516667.1:n.346-14_346-13insGTTGGGTGTG
XM_011518366.1:c.346-14_346-13insGTTGGGTGTG	XP_011516668.1:n.346-14_346-13insGTTGGGTGTG
XM_011518367.1:c.-111-14_-111-13insGTTGGGTGTG	XP_011516669.1:n.-111-14_-111-13insGTTGGGTGTG
XM_006717001.3:c.346-14_346-13insGTTGGGTGTG	XP_006717064.1:n.346-14_346-13insGTTGGGTGTG
XM_006717002.4:c.346-14_346-13insGTTGGGTGTG	XP_006717065.1:n.346-14_346-13insGTTGGGTGTG
XM_006717004.4:c.346-14_346-13insGTTGGGTGTG	XP_006717067.1:n.346-14_346-13insGTTGGGTGTG
XM_011518365.3:c.346-14_346-13insGTTGGGTGTG	XP_011516667.1:n.346-14_346-13insGTTGGGTGTG
XM_011518366.3:c.346-14_346-13insGTTGGGTGTG	XP_011516668.1:n.346-14_346-13insGTTGGGTGTG
XM_011518367.2:c.-111-14_-111-13insGTTGGGTGTG	XP_011516669.1:n.-111-14_-111-13insGTTGGGTGTG
XM_017014452.2:c.-111-14_-111-13insGTTGGGTGTG	XP_016869941.1:n.-111-14_-111-13insGTTGGGTGTG
XM_017014453.1:c.-111-14_-111-13insGTTGGGTGTG	XP_016869942.1:n.-111-14_-111-13insGTTGGGTGTG
XM_017014454.1:c.-111-14_-111-13insGTTGGGTGTG	XP_016869943.1:n.-111-14_-111-13insGTTGGGTGTG
XM_024447451.1:c.346-14_346-13insGTTGGGTGTG	XP_024303219.1:n.346-14_346-13insGTTGGGTGTG
NM_000136.3:c.346-14_346-13insGTTGGGTGTG MANE Select	NP_000127.2:n.346-14_346-13insGTTGGGTGTG
NM_001243743.2:c.346-14_346-13insGTTGGGTGTG	NP_001230672.1:n.346-14_346-13insGTTGGGTGTG
NM_001243744.2:c.346-14_346-13insGTTGGGTGTG	NP_001230673.1:n.346-14_346-13insGTTGGGTGTG