Canonical Allele Identifier: CA868770739

Gene: AOPEP FANCC

Linked Data

• dbSNP Id: rs1432442585
• gnomAD v4: 9-95110997-G-A
• MyVariant Identifiers: chr9:g.97873279G>A (hg19) ; chr9:g.95110997G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95110997G>A , CM000671.2:g.95110997G>A	GRCh38
NC_000009.11:g.97873279G>A , CM000671.1:g.97873279G>A	GRCh37
NC_000009.10:g.96913100G>A	NCBI36
NG_011707.1:g.211713C>T , LRG_497:g.211713C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+30217G>A (AOPEP)
ENST00000696260.1:n.2144+466C>T (FANCC)
ENST00000289081.8:c.1329+466C>T (FANCC) MANE Select	ENSP00000289081.3:n.1329+466C>T
ENST00000375305.6:c.1329+466C>T (FANCC)	ENSP00000364454.1:n.1329+466C>T
ENST00000490972.7:c.*199C>T (FANCC)	ENSP00000479931.1:n.*199C>T
ENST00000649334.1:c.1474+466C>T (FANCC)	ENSP00000497735.1:n.1474+466C>T
ENST00000289081.7:c.1329+466C>T (FANCC)	ENSP00000289081.3:n.1329+466C>T
ENST00000375305.5:c.1329+466C>T (FANCC)	ENSP00000364454.1:n.1329+466C>T
ENST00000464627.5:n.656+466C>T (FANCC)
ENST00000477942.5:n.684+466C>T (FANCC)
ENST00000480712.5:n.514+466C>T (FANCC)
ENST00000490972.6:c.*199C>T (FANCC)	ENSP00000479931.1:n.*199C>T
NM_000136.2:c.1329+466C>T , LRG_497t1:c.1329+466C>T (FANCC)	NP_000127.2:n.1329+466C>T
NM_001243743.1:c.1329+466C>T (FANCC)	NP_001230672.1:n.1329+466C>T
NM_001243744.1:c.*199C>T (FANCC)	NP_001230673.1:n.*199C>T
XM_005251802.2:c.648+466C>T (FANCC)	XP_005251859.1:n.648+466C>T
XM_006717001.1:c.1164+466C>T (FANCC)	XP_006717064.1:n.1164+466C>T
XM_006717002.2:c.1329+466C>T (FANCC)	XP_006717065.1:n.1329+466C>T
XM_011518365.1:c.1329+466C>T (FANCC)	XP_011516667.1:n.1329+466C>T
XM_011518367.1:c.873+466C>T (FANCC)	XP_011516669.1:n.873+466C>T
XM_011519121.1:c.2319+30217G>A (AOPEP)	XP_011517423.1:n.2319+30217G>A
XM_005251802.3:c.648+466C>T (FANCC)	XP_005251859.1:n.648+466C>T
XM_006717001.3:c.1164+466C>T (FANCC)	XP_006717064.1:n.1164+466C>T
XM_006717002.4:c.1329+466C>T (FANCC)	XP_006717065.1:n.1329+466C>T
XM_011518365.3:c.1329+466C>T (FANCC)	XP_011516667.1:n.1329+466C>T
XM_011518366.3:c.*314C>T (FANCC)	XP_011516668.1:n.*314C>T
XM_011518367.2:c.873+466C>T (FANCC)	XP_011516669.1:n.873+466C>T
XM_011519121.3:c.2319+30217G>A (AOPEP)	XP_011517423.1:n.2319+30217G>A
XM_017014452.2:c.873+466C>T (FANCC)	XP_016869941.1:n.873+466C>T
XM_017014453.1:c.873+466C>T (FANCC)	XP_016869942.1:n.873+466C>T
XM_017014454.1:c.708+466C>T (FANCC)	XP_016869943.1:n.708+466C>T
XM_024447451.1:c.1329+466C>T (FANCC)	XP_024303219.1:n.1329+466C>T
NM_000136.3:c.1329+466C>T (FANCC) MANE Select	NP_000127.2:n.1329+466C>T
NM_001243743.2:c.1329+466C>T (FANCC)	NP_001230672.1:n.1329+466C>T
NM_001243744.2:c.*199C>T (FANCC)	NP_001230673.1:n.*199C>T