Canonical Allele Identifier: CA868745276

Gene: FANCC

Linked Data

• dbSNP Id: rs1182677281
• gnomAD v3: 9-95172339-AAAG-A
• gnomAD v4: 9-95172339-AAAG-A
• MyVariant Identifiers: chr9:g.97934622_97934624del (hg19) ; chr9:g.95172340_95172342del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95172343_95172345del , CM000671.2:g.95172343_95172345del	GRCh38
NC_000009.11:g.97934625_97934627del , CM000671.1:g.97934625_97934627del	GRCh37
NC_000009.10:g.96974446_96974448del	NCBI36
NG_011707.1:g.150368_150370del , LRG_497:g.150368_150370del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.737-195_737-193del
ENST00000289081.8:c.346-195_346-193del MANE Select	ENSP00000289081.3:n.346-195_346-193del
ENST00000375305.6:c.346-195_346-193del	ENSP00000364454.1:n.346-195_346-193del
ENST00000490972.7:c.346-195_346-193del	ENSP00000479931.1:n.346-195_346-193del
ENST00000636777.1:n.404-195_404-193del
ENST00000647778.1:c.346-195_346-193del	ENSP00000498125.1:n.346-195_346-193del
ENST00000647882.1:c.346-195_346-193del	ENSP00000497025.1:n.346-195_346-193del
ENST00000649334.1:c.491-195_491-193del	ENSP00000497735.1:n.491-195_491-193del
ENST00000649701.1:n.61-195_61-193del
ENST00000289081.7:c.346-195_346-193del	ENSP00000289081.3:n.346-195_346-193del
ENST00000375305.5:c.346-195_346-193del	ENSP00000364454.1:n.346-195_346-193del
ENST00000433829.1:c.346-195_346-193del	ENSP00000406908.1:n.346-195_346-193del
ENST00000474949.1:n.703-195_703-193del
ENST00000490972.6:c.346-195_346-193del	ENSP00000479931.1:n.346-195_346-193del
NM_000136.2:c.346-195_346-193del , LRG_497t1:c.346-195_346-193del	NP_000127.2:n.346-195_346-193del
NM_001243743.1:c.346-195_346-193del	NP_001230672.1:n.346-195_346-193del
NM_001243744.1:c.346-195_346-193del	NP_001230673.1:n.346-195_346-193del
XM_006717001.1:c.346-195_346-193del	XP_006717064.1:n.346-195_346-193del
XM_006717002.2:c.346-195_346-193del	XP_006717065.1:n.346-195_346-193del
XM_006717004.2:c.346-195_346-193del	XP_006717067.1:n.346-195_346-193del
XM_011518365.1:c.346-195_346-193del	XP_011516667.1:n.346-195_346-193del
XM_011518366.1:c.346-195_346-193del	XP_011516668.1:n.346-195_346-193del
XM_011518367.1:c.-111-195_-111-193del	XP_011516669.1:n.-111-195_-111-193del
XM_006717001.3:c.346-195_346-193del	XP_006717064.1:n.346-195_346-193del
XM_006717002.4:c.346-195_346-193del	XP_006717065.1:n.346-195_346-193del
XM_006717004.4:c.346-195_346-193del	XP_006717067.1:n.346-195_346-193del
XM_011518365.3:c.346-195_346-193del	XP_011516667.1:n.346-195_346-193del
XM_011518366.3:c.346-195_346-193del	XP_011516668.1:n.346-195_346-193del
XM_011518367.2:c.-111-195_-111-193del	XP_011516669.1:n.-111-195_-111-193del
XM_017014452.2:c.-111-195_-111-193del	XP_016869941.1:n.-111-195_-111-193del
XM_017014453.1:c.-111-195_-111-193del	XP_016869942.1:n.-111-195_-111-193del
XM_017014454.1:c.-111-195_-111-193del	XP_016869943.1:n.-111-195_-111-193del
XM_024447451.1:c.346-195_346-193del	XP_024303219.1:n.346-195_346-193del
NM_000136.3:c.346-195_346-193del MANE Select	NP_000127.2:n.346-195_346-193del
NM_001243743.2:c.346-195_346-193del	NP_001230672.1:n.346-195_346-193del
NM_001243744.2:c.346-195_346-193del	NP_001230673.1:n.346-195_346-193del