Canonical Allele Identifier: CA159414

Gene: AOPEP FANCC

Linked Data

• ClinVar Variation Id: 134306
• ClinVar RCV Id: RCV000120980
• dbSNP Id: rs587778327
• MyVariant Identifiers: chr9:g.97912265C>A (hg19) ; chr9:g.95149983C>A (hg38)
• PubMed: PMID:24728327

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95149983C>A , CM000671.2:g.95149983C>A	GRCh38
NC_000009.11:g.97912265C>A , CM000671.1:g.97912265C>A	GRCh37
NC_000009.10:g.96952086C>A	NCBI36
NG_011707.1:g.172727G>T , LRG_497:g.172727G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.3183C>A (AOPEP)
ENST00000696261.1:n.1017G>T (FANCC)
ENST00000289081.8:c.626G>T (FANCC) MANE Select	ENSP00000289081.3:p.Arg209Leu
ENST00000375305.6:c.626G>T (FANCC)	ENSP00000364454.1:p.Arg209Leu
ENST00000490972.7:c.626G>T (FANCC)	ENSP00000479931.1:p.Arg209Leu
ENST00000649334.1:c.771G>T (FANCC)	ENSP00000497735.1:n.771G>T
ENST00000649701.1:n.341G>T (FANCC)
ENST00000289081.7:c.626G>T (FANCC)	ENSP00000289081.3:p.Arg209Leu
ENST00000375305.5:c.626G>T (FANCC)	ENSP00000364454.1:p.Arg209Leu
ENST00000490972.6:c.626G>T (FANCC)	ENSP00000479931.1:p.Arg209Leu
ENST00000493098.1:n.51G>T (FANCC)
NM_000136.2:c.626G>T , LRG_497t1:c.626G>T (FANCC)	NP_000127.2:p.Arg209Leu
NM_001243743.1:c.626G>T (FANCC)	NP_001230672.1:p.Arg209Leu
NM_001243744.1:c.626G>T (FANCC)	NP_001230673.1:p.Arg209Leu
XM_006717001.1:c.522-14481G>T (FANCC)	XP_006717064.1:n.522-14481G>T
XM_006717002.2:c.626G>T (FANCC)	XP_006717065.1:p.Arg209Leu
XM_006717004.2:c.626G>T (FANCC)	XP_006717067.1:p.Arg209Leu
XM_011518365.1:c.626G>T (FANCC)	XP_011516667.1:p.Arg209Leu
XM_011518366.1:c.626G>T (FANCC)	XP_011516668.1:p.Arg209Leu
XM_011518367.1:c.170G>T (FANCC)	XP_011516669.1:p.Arg57Leu
XM_006717001.3:c.522-14481G>T (FANCC)	XP_006717064.1:n.522-14481G>T
XM_006717002.4:c.626G>T (FANCC)	XP_006717065.1:p.Arg209Leu
XM_006717004.4:c.626G>T (FANCC)	XP_006717067.1:p.Arg209Leu
XM_011518365.3:c.626G>T (FANCC)	XP_011516667.1:p.Arg209Leu
XM_011518366.3:c.626G>T (FANCC)	XP_011516668.1:p.Arg209Leu
XM_011518367.2:c.170G>T (FANCC)	XP_011516669.1:p.Arg57Leu
XM_017014452.2:c.170G>T (FANCC)	XP_016869941.1:p.Arg57Leu
XM_017014453.1:c.170G>T (FANCC)	XP_016869942.1:p.Arg57Leu
XM_017014454.1:c.66-14481G>T (FANCC)	XP_016869943.1:n.66-14481G>T
XM_024447451.1:c.626G>T (FANCC)	XP_024303219.1:p.Arg209Leu
NM_000136.3:c.626G>T (FANCC) MANE Select	NP_000127.2:p.Arg209Leu
NM_001243743.2:c.626G>T (FANCC)	NP_001230672.1:p.Arg209Leu
NM_001243744.2:c.626G>T (FANCC)	NP_001230673.1:p.Arg209Leu