Canonical Allele Identifier: CA589489208

Gene: FANCC

Linked Data

• dbSNP Id: rs1486148240
• gnomAD v2: 9-97933456-C-CA
• gnomAD v4: 9-95171174-C-CA
• MyVariant Identifiers: chr9:g.97933456_97933457insA (hg19) ; chr9:g.95171174_95171175insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171175dup , CM000671.2:g.95171175dup	GRCh38
NC_000009.11:g.97933457dup , CM000671.1:g.97933457dup	GRCh37
NC_000009.10:g.96973278dup	NCBI36
NG_011707.1:g.151535dup , LRG_497:g.151535dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.848-32dup
ENST00000289081.8:c.457-32dup MANE Select	ENSP00000289081.3:n.457-32dup
ENST00000375305.6:c.457-32dup	ENSP00000364454.1:n.457-32dup
ENST00000490972.7:c.457-32dup	ENSP00000479931.1:n.457-32dup
ENST00000636777.1:n.515-32dup
ENST00000647778.1:c.457-32dup	ENSP00000498125.1:n.457-32dup
ENST00000649334.1:c.602-32dup	ENSP00000497735.1:n.602-32dup
ENST00000649701.1:n.172-32dup
ENST00000289081.7:c.457-32dup	ENSP00000289081.3:n.457-32dup
ENST00000375305.5:c.457-32dup	ENSP00000364454.1:n.457-32dup
ENST00000474949.1:n.814-32dup
ENST00000490972.6:c.457-32dup	ENSP00000479931.1:n.457-32dup
NM_000136.2:c.457-32dup , LRG_497t1:c.457-32dup	NP_000127.2:n.457-32dup
NM_001243743.1:c.457-32dup	NP_001230672.1:n.457-32dup
NM_001243744.1:c.457-32dup	NP_001230673.1:n.457-32dup
XM_006717001.1:c.457-32dup	XP_006717064.1:n.457-32dup
XM_006717002.2:c.457-32dup	XP_006717065.1:n.457-32dup
XM_006717004.2:c.457-32dup	XP_006717067.1:n.457-32dup
XM_011518365.1:c.457-32dup	XP_011516667.1:n.457-32dup
XM_011518366.1:c.457-32dup	XP_011516668.1:n.457-32dup
XM_011518367.1:c.1-32dup	XP_011516669.1:n.1-32dup
XM_006717001.3:c.457-32dup	XP_006717064.1:n.457-32dup
XM_006717002.4:c.457-32dup	XP_006717065.1:n.457-32dup
XM_006717004.4:c.457-32dup	XP_006717067.1:n.457-32dup
XM_011518365.3:c.457-32dup	XP_011516667.1:n.457-32dup
XM_011518366.3:c.457-32dup	XP_011516668.1:n.457-32dup
XM_011518367.2:c.1-32dup	XP_011516669.1:n.1-32dup
XM_017014452.2:c.1-32dup	XP_016869941.1:n.1-32dup
XM_017014453.1:c.1-32dup	XP_016869942.1:n.1-32dup
XM_017014454.1:c.1-32dup	XP_016869943.1:n.1-32dup
XM_024447451.1:c.457-32dup	XP_024303219.1:n.457-32dup
NM_000136.3:c.457-32dup MANE Select	NP_000127.2:n.457-32dup
NM_001243743.2:c.457-32dup	NP_001230672.1:n.457-32dup
NM_001243744.2:c.457-32dup	NP_001230673.1:n.457-32dup