Canonical Allele Identifier: CA374106265

Gene: AOPEP FANCC

Linked Data

• ClinVar Variation Id: 1770409
• ClinVar RCV Id: RCV002387757
• dbSNP Id: rs2134456702
• MyVariant Identifiers: chr9:g.97869538G>A (hg19) ; chr9:g.95107256G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107256G>A , CM000671.2:g.95107256G>A	GRCh38
NC_000009.11:g.97869538G>A , CM000671.1:g.97869538G>A	GRCh37
NC_000009.10:g.96909359G>A	NCBI36
NG_011707.1:g.215454C>T , LRG_497:g.215454C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000710812.1:n.410+26476G>A (AOPEP)
ENST00000696260.1:n.2158C>T (FANCC)
ENST00000289081.8:c.1343C>T (FANCC) MANE Select	ENSP00000289081.3:p.Ala448Val
ENST00000375305.6:c.1343C>T (FANCC)	ENSP00000364454.1:p.Ala448Val
ENST00000649334.1:c.1488C>T (FANCC)	ENSP00000497735.1:n.1488C>T
ENST00000289081.7:c.1343C>T (FANCC)	ENSP00000289081.3:p.Ala448Val
ENST00000375305.5:c.1343C>T (FANCC)	ENSP00000364454.1:p.Ala448Val
ENST00000464627.5:n.670C>T (FANCC)
NM_000136.2:c.1343C>T , LRG_497t1:c.1343C>T (FANCC)	NP_000127.2:p.Ala448Val
NM_001243743.1:c.1343C>T (FANCC)	NP_001230672.1:p.Ala448Val
XM_005251802.2:c.662C>T (FANCC)	XP_005251859.1:p.Ala221Val
XM_006717001.1:c.1178C>T (FANCC)	XP_006717064.1:p.Ala393Val
XM_011518365.1:c.1343C>T (FANCC)	XP_011516667.1:p.Ala448Val
XM_011518367.1:c.887C>T (FANCC)	XP_011516669.1:p.Ala296Val
XM_011519121.1:c.2319+26476G>A (AOPEP)	XP_011517423.1:n.2319+26476G>A
XM_005251802.3:c.662C>T (FANCC)	XP_005251859.1:p.Ala221Val
XM_006717001.3:c.1178C>T (FANCC)	XP_006717064.1:p.Ala393Val
XM_011518365.3:c.1343C>T (FANCC)	XP_011516667.1:p.Ala448Val
XM_011518367.2:c.887C>T (FANCC)	XP_011516669.1:p.Ala296Val
XM_011519121.3:c.2319+26476G>A (AOPEP)	XP_011517423.1:n.2319+26476G>A
XM_017014452.2:c.887C>T (FANCC)	XP_016869941.1:p.Ala296Val
XM_017014453.1:c.887C>T (FANCC)	XP_016869942.1:p.Ala296Val
XM_017014454.1:c.722C>T (FANCC)	XP_016869943.1:p.Ala241Val
XM_024447451.1:c.1343C>T (FANCC)	XP_024303219.1:p.Ala448Val
XR_001746847.1:n.674G>A
NM_000136.3:c.1343C>T (FANCC) MANE Select	NP_000127.2:p.Ala448Val
NM_001243743.2:c.1343C>T (FANCC)	NP_001230672.1:p.Ala448Val