Canonical Allele Identifier: CA2690792965

Gene: FANCC

Linked Data

• gnomAD v4: 9-95249478-C-CCATGCTA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95249478_95249479insCATGCTA , CM000671.2:g.95249478_95249479insCATGCTA	GRCh38
NC_000009.11:g.98011760_98011761insCATGCTA , CM000671.1:g.98011760_98011761insCATGCTA	GRCh37
NC_000009.10:g.97051581_97051582insCATGCTA	NCBI36
NG_011707.1:g.73231_73232insTAGCATG , LRG_497:g.73231_73232insTAGCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.169-110_169-109insTAGCATG
ENST00000696262.1:c.-78-110_-78-109insTAGCATG	ENSP00000512510.1:n.-78-110_-78-109insTAGCATG
ENST00000696263.1:n.178-110_178-109insTAGCATG
ENST00000289081.8:c.-78-110_-78-109insTAGCATG MANE Select	ENSP00000289081.3:n.-78-110_-78-109insTAGCATG
ENST00000375305.6:c.-78-110_-78-109insTAGCATG	ENSP00000364454.1:n.-78-110_-78-109insTAGCATG
ENST00000490972.7:c.-78-110_-78-109insTAGCATG	ENSP00000479931.1:n.-78-110_-78-109insTAGCATG
ENST00000636777.1:n.20-149_20-148insTAGCATG
ENST00000647778.1:c.-78-110_-78-109insTAGCATG	ENSP00000498125.1:n.-78-110_-78-109insTAGCATG
ENST00000647882.1:c.-78-110_-78-109insTAGCATG	ENSP00000497025.1:n.-78-110_-78-109insTAGCATG
ENST00000648415.1:n.1561-110_1561-109insTAGCATG
ENST00000649519.1:c.-78-110_-78-109insTAGCATG	ENSP00000497630.1:n.-78-110_-78-109insTAGCATG
ENST00000649611.1:c.-78-110_-78-109insTAGCATG	ENSP00000497986.1:n.-78-110_-78-109insTAGCATG
ENST00000650176.1:n.103-110_103-109insTAGCATG
ENST00000289081.7:c.-78-110_-78-109insTAGCATG	ENSP00000289081.3:n.-78-110_-78-109insTAGCATG
ENST00000375305.5:c.-78-110_-78-109insTAGCATG	ENSP00000364454.1:n.-78-110_-78-109insTAGCATG
ENST00000433829.1:c.-78-110_-78-109insTAGCATG	ENSP00000406908.1:n.-78-110_-78-109insTAGCATG
ENST00000474949.1:n.185-110_185-109insTAGCATG
ENST00000490972.6:c.-78-110_-78-109insTAGCATG	ENSP00000479931.1:n.-78-110_-78-109insTAGCATG
NM_000136.2:c.-78-110_-78-109insTAGCATG , LRG_497t1:c.-78-110_-78-109insTAGCATG	NP_000127.2:n.-78-110_-78-109insTAGCATG
NM_001243743.1:c.-78-110_-78-109insTAGCATG	NP_001230672.1:n.-78-110_-78-109insTAGCATG
NM_001243744.1:c.-78-110_-78-109insTAGCATG	NP_001230673.1:n.-78-110_-78-109insTAGCATG
XM_006717001.1:c.-78-110_-78-109insTAGCATG	XP_006717064.1:n.-78-110_-78-109insTAGCATG
XM_006717002.2:c.-78-110_-78-109insTAGCATG	XP_006717065.1:n.-78-110_-78-109insTAGCATG
XM_006717004.2:c.-78-110_-78-109insTAGCATG	XP_006717067.1:n.-78-110_-78-109insTAGCATG
XM_011518365.1:c.-78-110_-78-109insTAGCATG	XP_011516667.1:n.-78-110_-78-109insTAGCATG
XM_011518366.1:c.-78-110_-78-109insTAGCATG	XP_011516668.1:n.-78-110_-78-109insTAGCATG
XM_011518367.1:c.-679-110_-679-109insTAGCATG	XP_011516669.1:n.-679-110_-679-109insTAGCATG
XM_006717001.3:c.-78-110_-78-109insTAGCATG	XP_006717064.1:n.-78-110_-78-109insTAGCATG
XM_006717002.4:c.-78-110_-78-109insTAGCATG	XP_006717065.1:n.-78-110_-78-109insTAGCATG
XM_006717004.4:c.-78-110_-78-109insTAGCATG	XP_006717067.1:n.-78-110_-78-109insTAGCATG
XM_011518365.3:c.-78-110_-78-109insTAGCATG	XP_011516667.1:n.-78-110_-78-109insTAGCATG
XM_011518366.3:c.-78-110_-78-109insTAGCATG	XP_011516668.1:n.-78-110_-78-109insTAGCATG
XM_011518367.2:c.-679-110_-679-109insTAGCATG	XP_011516669.1:n.-679-110_-679-109insTAGCATG
XM_017014452.2:c.-679-110_-679-109insTAGCATG	XP_016869941.1:n.-679-110_-679-109insTAGCATG
XM_017014453.1:c.-679-110_-679-109insTAGCATG	XP_016869942.1:n.-679-110_-679-109insTAGCATG
XM_017014454.1:c.-679-110_-679-109insTAGCATG	XP_016869943.1:n.-679-110_-679-109insTAGCATG
XM_024447451.1:c.-78-110_-78-109insTAGCATG	XP_024303219.1:n.-78-110_-78-109insTAGCATG
NM_000136.3:c.-78-110_-78-109insTAGCATG MANE Select	NP_000127.2:n.-78-110_-78-109insTAGCATG
NM_001243743.2:c.-78-110_-78-109insTAGCATG	NP_001230672.1:n.-78-110_-78-109insTAGCATG
NM_001243744.2:c.-78-110_-78-109insTAGCATG	NP_001230673.1:n.-78-110_-78-109insTAGCATG