Canonical Allele Identifier: CA374107390

Gene: AOPEP FANCC

Linked Data

• ClinVar Variation Id: 1898849
• ClinVar RCV Id: RCV002570160 ; RCV003164778
• dbSNP Id: rs1381182324
• gnomAD v3: 9-95111549-C-T
• gnomAD v4: 9-95111549-C-T
• MyVariant Identifiers: chr9:g.97873831C>T (hg19) ; chr9:g.95111549C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95111549C>T , CM000671.2:g.95111549C>T	GRCh38
NC_000009.11:g.97873831C>T , CM000671.1:g.97873831C>T	GRCh37
NC_000009.10:g.96913652C>T	NCBI36
NG_011707.1:g.211161G>A , LRG_497:g.211161G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+30769C>T (AOPEP)
ENST00000696260.1:n.2058G>A (FANCC)
ENST00000289081.8:c.1243G>A (FANCC) MANE Select	ENSP00000289081.3:p.Ala415Thr
ENST00000375305.6:c.1243G>A (FANCC)	ENSP00000364454.1:p.Ala415Thr
ENST00000490972.7:c.1243G>A (FANCC)	ENSP00000479931.1:p.Ala415Thr
ENST00000649334.1:c.1388G>A (FANCC)	ENSP00000497735.1:n.1388G>A
ENST00000289081.7:c.1243G>A (FANCC)	ENSP00000289081.3:p.Ala415Thr
ENST00000375305.5:c.1243G>A (FANCC)	ENSP00000364454.1:p.Ala415Thr
ENST00000464627.5:n.570G>A (FANCC)
ENST00000477942.5:n.598G>A (FANCC)
ENST00000480712.5:n.428G>A (FANCC)
ENST00000490972.6:c.1243G>A (FANCC)	ENSP00000479931.1:p.Ala415Thr
NM_000136.2:c.1243G>A , LRG_497t1:c.1243G>A (FANCC)	NP_000127.2:p.Ala415Thr
NM_001243743.1:c.1243G>A (FANCC)	NP_001230672.1:p.Ala415Thr
NM_001243744.1:c.1243G>A (FANCC)	NP_001230673.1:p.Ala415Thr
XM_005251802.2:c.562G>A (FANCC)	XP_005251859.1:p.Ala188Thr
XM_006717001.1:c.1078G>A (FANCC)	XP_006717064.1:p.Ala360Thr
XM_006717002.2:c.1243G>A (FANCC)	XP_006717065.1:p.Ala415Thr
XM_006717004.2:c.*138G>A (FANCC)	XP_006717067.1:n.*138G>A
XM_011518365.1:c.1243G>A (FANCC)	XP_011516667.1:p.Ala415Thr
XM_011518366.1:c.1243G>A (FANCC)	XP_011516668.1:p.Ala415Thr
XM_011518367.1:c.787G>A (FANCC)	XP_011516669.1:p.Ala263Thr
XM_011519121.1:c.2319+30769C>T (AOPEP)	XP_011517423.1:n.2319+30769C>T
XM_005251802.3:c.562G>A (FANCC)	XP_005251859.1:p.Ala188Thr
XM_006717001.3:c.1078G>A (FANCC)	XP_006717064.1:p.Ala360Thr
XM_006717002.4:c.1243G>A (FANCC)	XP_006717065.1:p.Ala415Thr
XM_006717004.4:c.*138G>A (FANCC)	XP_006717067.1:n.*138G>A
XM_011518365.3:c.1243G>A (FANCC)	XP_011516667.1:p.Ala415Thr
XM_011518366.3:c.1243G>A (FANCC)	XP_011516668.1:p.Ala415Thr
XM_011518367.2:c.787G>A (FANCC)	XP_011516669.1:p.Ala263Thr
XM_011519121.3:c.2319+30769C>T (AOPEP)	XP_011517423.1:n.2319+30769C>T
XM_017014452.2:c.787G>A (FANCC)	XP_016869941.1:p.Ala263Thr
XM_017014453.1:c.787G>A (FANCC)	XP_016869942.1:p.Ala263Thr
XM_017014454.1:c.622G>A (FANCC)	XP_016869943.1:p.Ala208Thr
XM_024447451.1:c.1243G>A (FANCC)	XP_024303219.1:p.Ala415Thr
NM_000136.3:c.1243G>A (FANCC) MANE Select	NP_000127.2:p.Ala415Thr
NM_001243743.2:c.1243G>A (FANCC)	NP_001230672.1:p.Ala415Thr
NM_001243744.2:c.1243G>A (FANCC)	NP_001230673.1:p.Ala415Thr