Canonical Allele Identifier: CA2690792860

Gene: FANCC

Linked Data

• gnomAD v4: 9-95249310-G-GTGATA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95249314_95249315insATGAT , CM000671.2:g.95249314_95249315insATGAT	GRCh38
NC_000009.11:g.98011596_98011597insATGAT , CM000671.1:g.98011596_98011597insATGAT	GRCh37
NC_000009.10:g.97051417_97051418insATGAT	NCBI36
NG_011707.1:g.73399_73400insTATCA , LRG_497:g.73399_73400insTATCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.227_228insTATCA
ENST00000696262.1:c.-20_-19insTATCA	ENSP00000512510.1:n.-20_-19insTATCA
ENST00000696263.1:n.236_237insTATCA
ENST00000289081.8:c.-20_-19insTATCA MANE Select	ENSP00000289081.3:n.-20_-19insTATCA
ENST00000375305.6:c.-20_-19insTATCA	ENSP00000364454.1:n.-20_-19insTATCA
ENST00000490972.7:c.-20_-19insTATCA	ENSP00000479931.1:n.-20_-19insTATCA
ENST00000636777.1:n.39_40insTATCA
ENST00000647778.1:c.-20_-19insTATCA	ENSP00000498125.1:n.-20_-19insTATCA
ENST00000647882.1:c.-20_-19insTATCA	ENSP00000497025.1:n.-20_-19insTATCA
ENST00000648415.1:n.1619_1620insTATCA
ENST00000649519.1:c.-20_-19insTATCA	ENSP00000497630.1:n.-20_-19insTATCA
ENST00000649611.1:c.-20_-19insTATCA	ENSP00000497986.1:n.-20_-19insTATCA
ENST00000650176.1:n.161_162insTATCA
ENST00000289081.7:c.-20_-19insTATCA	ENSP00000289081.3:n.-20_-19insTATCA
ENST00000375305.5:c.-20_-19insTATCA	ENSP00000364454.1:n.-20_-19insTATCA
ENST00000433829.1:c.-20_-19insTATCA	ENSP00000406908.1:n.-20_-19insTATCA
ENST00000474949.1:n.243_244insTATCA
ENST00000490972.6:c.-20_-19insTATCA	ENSP00000479931.1:n.-20_-19insTATCA
NM_000136.2:c.-20_-19insTATCA , LRG_497t1:c.-20_-19insTATCA	NP_000127.2:n.-20_-19insTATCA
NM_001243743.1:c.-20_-19insTATCA	NP_001230672.1:n.-20_-19insTATCA
NM_001243744.1:c.-20_-19insTATCA	NP_001230673.1:n.-20_-19insTATCA
XM_006717001.1:c.-20_-19insTATCA	XP_006717064.1:n.-20_-19insTATCA
XM_006717002.2:c.-20_-19insTATCA	XP_006717065.1:n.-20_-19insTATCA
XM_006717004.2:c.-20_-19insTATCA	XP_006717067.1:n.-20_-19insTATCA
XM_011518365.1:c.-20_-19insTATCA	XP_011516667.1:n.-20_-19insTATCA
XM_011518366.1:c.-20_-19insTATCA	XP_011516668.1:n.-20_-19insTATCA
XM_011518367.1:c.-621_-620insTATCA	XP_011516669.1:n.-621_-620insTATCA
XM_006717001.3:c.-20_-19insTATCA	XP_006717064.1:n.-20_-19insTATCA
XM_006717002.4:c.-20_-19insTATCA	XP_006717065.1:n.-20_-19insTATCA
XM_006717004.4:c.-20_-19insTATCA	XP_006717067.1:n.-20_-19insTATCA
XM_011518365.3:c.-20_-19insTATCA	XP_011516667.1:n.-20_-19insTATCA
XM_011518366.3:c.-20_-19insTATCA	XP_011516668.1:n.-20_-19insTATCA
XM_011518367.2:c.-621_-620insTATCA	XP_011516669.1:n.-621_-620insTATCA
XM_017014452.2:c.-621_-620insTATCA	XP_016869941.1:n.-621_-620insTATCA
XM_017014453.1:c.-621_-620insTATCA	XP_016869942.1:n.-621_-620insTATCA
XM_017014454.1:c.-621_-620insTATCA	XP_016869943.1:n.-621_-620insTATCA
XM_024447451.1:c.-20_-19insTATCA	XP_024303219.1:n.-20_-19insTATCA
NM_000136.3:c.-20_-19insTATCA MANE Select	NP_000127.2:n.-20_-19insTATCA
NM_001243743.2:c.-20_-19insTATCA	NP_001230672.1:n.-20_-19insTATCA
NM_001243744.2:c.-20_-19insTATCA	NP_001230673.1:n.-20_-19insTATCA