Canonical Allele Identifier: CA5137728

Gene: FANCC

Linked Data

• ClinVar Variation Id: 570343
• ClinVar RCV Id: RCV000691188
• dbSNP Id: rs763416214
• ExAC: 9:97933434 CA / C
• gnomAD v2: 9-97933434-CA-C
• gnomAD v4: 9-95171152-CA-C
• MyVariant Identifiers: chr9:g.97933435del (hg19) ; chr9:g.95171153del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171156del , CM000671.2:g.95171156del	GRCh38
NC_000009.11:g.97933438del , CM000671.1:g.97933438del	GRCh37
NC_000009.10:g.96973259del	NCBI36
NG_011707.1:g.151557del , LRG_497:g.151557del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.848-10del
ENST00000289081.8:c.457-10del MANE Select	ENSP00000289081.3:n.457-10del
ENST00000375305.6:c.457-10del	ENSP00000364454.1:n.457-10del
ENST00000490972.7:c.457-10del	ENSP00000479931.1:n.457-10del
ENST00000636777.1:n.515-10del
ENST00000647778.1:c.457-10del	ENSP00000498125.1:n.457-10del
ENST00000649334.1:c.602-10del	ENSP00000497735.1:n.602-10del
ENST00000649701.1:n.172-10del
ENST00000289081.7:c.457-10del	ENSP00000289081.3:n.457-10del
ENST00000375305.5:c.457-10del	ENSP00000364454.1:n.457-10del
ENST00000474949.1:n.814-10del
ENST00000490972.6:c.457-10del	ENSP00000479931.1:n.457-10del
NM_000136.2:c.457-10del , LRG_497t1:c.457-10del	NP_000127.2:n.457-10del
NM_001243743.1:c.457-10del	NP_001230672.1:n.457-10del
NM_001243744.1:c.457-10del	NP_001230673.1:n.457-10del
XM_006717001.1:c.457-10del	XP_006717064.1:n.457-10del
XM_006717002.2:c.457-10del	XP_006717065.1:n.457-10del
XM_006717004.2:c.457-10del	XP_006717067.1:n.457-10del
XM_011518365.1:c.457-10del	XP_011516667.1:n.457-10del
XM_011518366.1:c.457-10del	XP_011516668.1:n.457-10del
XM_011518367.1:c.1-10del	XP_011516669.1:n.1-10del
XM_006717001.3:c.457-10del	XP_006717064.1:n.457-10del
XM_006717002.4:c.457-10del	XP_006717065.1:n.457-10del
XM_006717004.4:c.457-10del	XP_006717067.1:n.457-10del
XM_011518365.3:c.457-10del	XP_011516667.1:n.457-10del
XM_011518366.3:c.457-10del	XP_011516668.1:n.457-10del
XM_011518367.2:c.1-10del	XP_011516669.1:n.1-10del
XM_017014452.2:c.1-10del	XP_016869941.1:n.1-10del
XM_017014453.1:c.1-10del	XP_016869942.1:n.1-10del
XM_017014454.1:c.1-10del	XP_016869943.1:n.1-10del
XM_024447451.1:c.457-10del	XP_024303219.1:n.457-10del
NM_000136.3:c.457-10del MANE Select	NP_000127.2:n.457-10del
NM_001243743.2:c.457-10del	NP_001230672.1:n.457-10del
NM_001243744.2:c.457-10del	NP_001230673.1:n.457-10del