Canonical Allele Identifier: CA2695201606

Gene: AOPEP FANCC

Linked Data

• ClinVar Variation Id: 2675480
• ClinVar RCV Id: RCV003460187

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95111463del , CM000671.2:g.95111463del	GRCh38
NC_000009.11:g.97873745del , CM000671.1:g.97873745del	GRCh37
NC_000009.10:g.96913566del	NCBI36
NG_011707.1:g.211248del , LRG_497:g.211248del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+30683del (AOPEP)
ENST00000696260.1:n.2144+1del (FANCC)
ENST00000289081.8:c.1329+1del (FANCC)
ENST00000375305.6:c.1329+1del (FANCC)
ENST00000490972.7:c.1329+1del (FANCC)
ENST00000649334.1:c.1474+1del (FANCC)
ENST00000289081.7:c.1329+1del (FANCC)
ENST00000375305.5:c.1329+1del (FANCC)
ENST00000464627.5:n.656+1del (FANCC)
ENST00000477942.5:n.684+1del (FANCC)
ENST00000480712.5:n.514+1del (FANCC)
ENST00000490972.6:c.1329+1del (FANCC)
NM_000136.2:c.1329+1del , LRG_497t1:c.1329+1del (FANCC)
NM_001243743.1:c.1329+1del (FANCC)
NM_001243744.1:c.1329+1del (FANCC)
XM_005251802.2:c.648+1del (FANCC)
XM_006717001.1:c.1164+1del (FANCC)
XM_006717002.2:c.1329+1del (FANCC)
XM_011518365.1:c.1329+1del (FANCC)
XM_011518366.1:c.1329+1del (FANCC)
XM_011518367.1:c.873+1del (FANCC)
XM_011519121.1:c.2319+30683del (AOPEP)	XP_011517423.1:n.2319+30683del
XM_005251802.3:c.648+1del (FANCC)
XM_006717001.3:c.1164+1del (FANCC)
XM_006717002.4:c.1329+1del (FANCC)
XM_011518365.3:c.1329+1del (FANCC)
XM_011518366.3:c.1329+1del (FANCC)
XM_011518367.2:c.873+1del (FANCC)
XM_011519121.3:c.2319+30683del (AOPEP)	XP_011517423.1:n.2319+30683del
XM_017014452.2:c.873+1del (FANCC)
XM_017014453.1:c.873+1del (FANCC)
XM_017014454.1:c.708+1del (FANCC)
XM_024447451.1:c.1329+1del (FANCC)
NM_000136.3:c.1329+1del (FANCC)
NM_001243743.2:c.1329+1del (FANCC)
NM_001243744.2:c.1329+1del (FANCC)