Canonical Allele Identifier: CA196562397

Gene: AOPEP FANCC

Linked Data

• dbSNP Id: rs773560419
• gnomAD v2: 9-97897467-CTA-C
• gnomAD v3: 9-95135185-CTA-C
• gnomAD v4: 9-95135185-CTA-C
• MyVariant Identifiers: chr9:g.97897468_97897469del (hg19) ; chr9:g.95135186_95135187del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95135187_95135188del , CM000671.2:g.95135187_95135188del	GRCh38
NC_000009.11:g.97897469_97897470del , CM000671.1:g.97897469_97897470del	GRCh37
NC_000009.10:g.96937290_96937291del	NCBI36
NG_011707.1:g.187523_187524del , LRG_497:g.187523_187524del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.411-12024_411-12023del (AOPEP)
ENST00000696261.1:n.1393_1394del (FANCC)
ENST00000289081.8:c.843+159_843+160del (FANCC) MANE Select	ENSP00000289081.3:n.843+159_843+160del
ENST00000375305.6:c.843+159_843+160del (FANCC)	ENSP00000364454.1:n.843+159_843+160del
ENST00000490972.7:c.843+159_843+160del (FANCC)	ENSP00000479931.1:n.843+159_843+160del
ENST00000649334.1:c.988+159_988+160del (FANCC)	ENSP00000497735.1:n.988+159_988+160del
ENST00000649701.1:n.558+159_558+160del (FANCC)
ENST00000289081.7:c.843+159_843+160del (FANCC)	ENSP00000289081.3:n.843+159_843+160del
ENST00000375305.5:c.843+159_843+160del (FANCC)	ENSP00000364454.1:n.843+159_843+160del
ENST00000477942.5:n.198+159_198+160del (FANCC)
ENST00000480712.5:n.28+159_28+160del (FANCC)
ENST00000490972.6:c.843+159_843+160del (FANCC)	ENSP00000479931.1:n.843+159_843+160del
NM_000136.2:c.843+159_843+160del , LRG_497t1:c.843+159_843+160del (FANCC)	NP_000127.2:n.843+159_843+160del
NM_001243743.1:c.843+159_843+160del (FANCC)	NP_001230672.1:n.843+159_843+160del
NM_001243744.1:c.843+159_843+160del (FANCC)	NP_001230673.1:n.843+159_843+160del
XM_005251802.2:c.162+159_162+160del (FANCC)	XP_005251859.1:n.162+159_162+160del
XM_006717001.1:c.678+159_678+160del (FANCC)	XP_006717064.1:n.678+159_678+160del
XM_006717002.2:c.843+159_843+160del (FANCC)	XP_006717065.1:n.843+159_843+160del
XM_006717004.2:c.843+159_843+160del (FANCC)	XP_006717067.1:n.843+159_843+160del
XM_011518365.1:c.843+159_843+160del (FANCC)	XP_011516667.1:n.843+159_843+160del
XM_011518366.1:c.843+159_843+160del (FANCC)	XP_011516668.1:n.843+159_843+160del
XM_011518367.1:c.387+159_387+160del (FANCC)	XP_011516669.1:n.387+159_387+160del
XM_011519121.1:c.2320-12024_2320-12023del (AOPEP)	XP_011517423.1:n.2320-12024_2320-12023del
XM_005251802.3:c.162+159_162+160del (FANCC)	XP_005251859.1:n.162+159_162+160del
XM_006717001.3:c.678+159_678+160del (FANCC)	XP_006717064.1:n.678+159_678+160del
XM_006717002.4:c.843+159_843+160del (FANCC)	XP_006717065.1:n.843+159_843+160del
XM_006717004.4:c.843+159_843+160del (FANCC)	XP_006717067.1:n.843+159_843+160del
XM_011518365.3:c.843+159_843+160del (FANCC)	XP_011516667.1:n.843+159_843+160del
XM_011518366.3:c.843+159_843+160del (FANCC)	XP_011516668.1:n.843+159_843+160del
XM_011518367.2:c.387+159_387+160del (FANCC)	XP_011516669.1:n.387+159_387+160del
XM_011519121.3:c.2320-12024_2320-12023del (AOPEP)	XP_011517423.1:n.2320-12024_2320-12023del
XM_017014452.2:c.387+159_387+160del (FANCC)	XP_016869941.1:n.387+159_387+160del
XM_017014453.1:c.387+159_387+160del (FANCC)	XP_016869942.1:n.387+159_387+160del
XM_017014454.1:c.222+159_222+160del (FANCC)	XP_016869943.1:n.222+159_222+160del
XM_024447451.1:c.843+159_843+160del (FANCC)	XP_024303219.1:n.843+159_843+160del
NM_000136.3:c.843+159_843+160del (FANCC) MANE Select	NP_000127.2:n.843+159_843+160del
NM_001243743.2:c.843+159_843+160del (FANCC)	NP_001230672.1:n.843+159_843+160del
NM_001243744.2:c.843+159_843+160del (FANCC)	NP_001230673.1:n.843+159_843+160del