Canonical Allele Identifier: CA16041351

Gene: FANCC

Linked Data

• ClinVar Variation Id: 371370
• ClinVar RCV Id: RCV002436231 ; RCV003522962
• dbSNP Id: rs1057517219
• MyVariant Identifiers: chr9:g.98003027T>G (hg19) ; chr9:g.95240745T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95240745T>G , CM000671.2:g.95240745T>G	GRCh38
NC_000009.11:g.98003027T>G , CM000671.1:g.98003027T>G	GRCh37
NC_000009.10:g.97042848T>G	NCBI36
NG_011707.1:g.81965A>C , LRG_497:g.81965A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696261.1:n.497-2A>C
ENST00000696262.1:c.251-2A>C	ENSP00000512510.1:n.251-2A>C
ENST00000289081.8:c.251-2A>C MANE Select	ENSP00000289081.3:n.251-2A>C
ENST00000375305.6:c.251-2A>C	ENSP00000364454.1:n.251-2A>C
ENST00000490972.7:c.251-2A>C	ENSP00000479931.1:n.251-2A>C
ENST00000636777.1:n.309-2A>C
ENST00000647778.1:c.251-2A>C	ENSP00000498125.1:n.251-2A>C
ENST00000647882.1:c.251-2A>C	ENSP00000497025.1:n.251-2A>C
ENST00000648415.1:n.1889-2A>C
ENST00000649334.1:c.251-2A>C	ENSP00000497735.1:n.251-2A>C
ENST00000649519.1:c.251-2A>C	ENSP00000497630.1:n.251-2A>C
ENST00000649872.1:c.251-2A>C	ENSP00000497195.1:n.251-2A>C
ENST00000650176.1:n.431-2A>C
ENST00000289081.7:c.251-2A>C	ENSP00000289081.3:n.251-2A>C
ENST00000375305.5:c.251-2A>C	ENSP00000364454.1:n.251-2A>C
ENST00000433829.1:c.251-2A>C	ENSP00000406908.1:n.251-2A>C
ENST00000474949.1:n.513-2A>C
ENST00000490972.6:c.251-2A>C	ENSP00000479931.1:n.251-2A>C
NM_000136.2:c.251-2A>C , LRG_497t1:c.251-2A>C	NP_000127.2:n.251-2A>C
NM_001243743.1:c.251-2A>C	NP_001230672.1:n.251-2A>C
NM_001243744.1:c.251-2A>C	NP_001230673.1:n.251-2A>C
XM_006717001.1:c.251-2A>C	XP_006717064.1:n.251-2A>C
XM_006717002.2:c.251-2A>C	XP_006717065.1:n.251-2A>C
XM_006717004.2:c.251-2A>C	XP_006717067.1:n.251-2A>C
XM_011518365.1:c.251-2A>C	XP_011516667.1:n.251-2A>C
XM_011518366.1:c.251-2A>C	XP_011516668.1:n.251-2A>C
XM_011518367.1:c.-351-2A>C	XP_011516669.1:n.-351-2A>C
XM_006717001.3:c.251-2A>C	XP_006717064.1:n.251-2A>C
XM_006717002.4:c.251-2A>C	XP_006717065.1:n.251-2A>C
XM_006717004.4:c.251-2A>C	XP_006717067.1:n.251-2A>C
XM_011518365.3:c.251-2A>C	XP_011516667.1:n.251-2A>C
XM_011518366.3:c.251-2A>C	XP_011516668.1:n.251-2A>C
XM_011518367.2:c.-351-2A>C	XP_011516669.1:n.-351-2A>C
XM_017014452.2:c.-351-2A>C	XP_016869941.1:n.-351-2A>C
XM_017014453.1:c.-351-2A>C	XP_016869942.1:n.-351-2A>C
XM_017014454.1:c.-351-2A>C	XP_016869943.1:n.-351-2A>C
XM_024447451.1:c.251-2A>C	XP_024303219.1:n.251-2A>C
NM_000136.3:c.251-2A>C MANE Select	NP_000127.2:n.251-2A>C
NM_001243743.2:c.251-2A>C	NP_001230672.1:n.251-2A>C
NM_001243744.2:c.251-2A>C	NP_001230673.1:n.251-2A>C