Canonical Allele Identifier: CA374105604

Gene: AOPEP FANCC

Linked Data

• ClinVar Variation Id: 3230365
• ClinVar RCV Id: RCV004520516
• gnomAD v4: 9-95107101-C-T
• MyVariant Identifiers: chr9:g.97869383C>T (hg19) ; chr9:g.95107101C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107101C>T , CM000671.2:g.95107101C>T	GRCh38
NC_000009.11:g.97869383C>T , CM000671.1:g.97869383C>T	GRCh37
NC_000009.10:g.96909204C>T	NCBI36
NG_011707.1:g.215609G>A , LRG_497:g.215609G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+26321C>T (AOPEP)
ENST00000696260.1:n.2313G>A (FANCC)
ENST00000289081.8:c.1498G>A (FANCC) MANE Select	ENSP00000289081.3:p.Gly500Arg
ENST00000375305.6:c.1498G>A (FANCC)	ENSP00000364454.1:p.Gly500Arg
ENST00000649334.1:c.1643G>A (FANCC)	ENSP00000497735.1:n.1643G>A
ENST00000289081.7:c.1498G>A (FANCC)	ENSP00000289081.3:p.Gly500Arg
ENST00000375305.5:c.1498G>A (FANCC)	ENSP00000364454.1:p.Gly500Arg
ENST00000464627.5:n.825G>A (FANCC)
NM_000136.2:c.1498G>A , LRG_497t1:c.1498G>A (FANCC)	NP_000127.2:p.Gly500Arg
NM_001243743.1:c.1498G>A (FANCC)	NP_001230672.1:p.Gly500Arg
XM_005251802.2:c.817G>A (FANCC)	XP_005251859.1:p.Gly273Arg
XM_006717001.1:c.1333G>A (FANCC)	XP_006717064.1:p.Gly445Arg
XM_011518365.1:c.1498G>A (FANCC)	XP_011516667.1:p.Gly500Arg
XM_011518367.1:c.1042G>A (FANCC)	XP_011516669.1:p.Gly348Arg
XM_011519121.1:c.2319+26321C>T (AOPEP)	XP_011517423.1:n.2319+26321C>T
XM_005251802.3:c.817G>A (FANCC)	XP_005251859.1:p.Gly273Arg
XM_006717001.3:c.1333G>A (FANCC)	XP_006717064.1:p.Gly445Arg
XM_011518365.3:c.1498G>A (FANCC)	XP_011516667.1:p.Gly500Arg
XM_011518367.2:c.1042G>A (FANCC)	XP_011516669.1:p.Gly348Arg
XM_011519121.3:c.2319+26321C>T (AOPEP)	XP_011517423.1:n.2319+26321C>T
XM_017014452.2:c.1042G>A (FANCC)	XP_016869941.1:p.Gly348Arg
XM_017014453.1:c.1042G>A (FANCC)	XP_016869942.1:p.Gly348Arg
XM_017014454.1:c.877G>A (FANCC)	XP_016869943.1:p.Gly293Arg
XM_024447451.1:c.1498G>A (FANCC)	XP_024303219.1:p.Gly500Arg
XR_001746847.1:n.519C>T
NM_000136.3:c.1498G>A (FANCC) MANE Select	NP_000127.2:p.Gly500Arg
NM_001243743.2:c.1498G>A (FANCC)	NP_001230672.1:p.Gly500Arg