Canonical Allele Identifier: CA918511979

Gene: AOPEP FANCC

Linked Data

• dbSNP Id: rs1588049257

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95111796_95111800del , CM000671.2:g.95111796_95111800del	GRCh38
NC_000009.11:g.97874078_97874082del , CM000671.1:g.97874078_97874082del	GRCh37
NC_000009.10:g.96913899_96913903del	NCBI36
NG_011707.1:g.210911_210915del , LRG_497:g.210911_210915del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+31016_410+31020del (AOPEP)
ENST00000696260.1:n.1808_1812del (FANCC)
ENST00000289081.8:c.1155-162_1155-158del (FANCC) MANE Select	ENSP00000289081.3:n.1155-162_1155-158del
ENST00000375305.6:c.1155-162_1155-158del (FANCC)	ENSP00000364454.1:n.1155-162_1155-158del
ENST00000490972.7:c.1155-162_1155-158del (FANCC)	ENSP00000479931.1:n.1155-162_1155-158del
ENST00000649334.1:c.1300-162_1300-158del (FANCC)	ENSP00000497735.1:n.1300-162_1300-158del
ENST00000289081.7:c.1155-162_1155-158del (FANCC)	ENSP00000289081.3:n.1155-162_1155-158del
ENST00000375305.5:c.1155-162_1155-158del (FANCC)	ENSP00000364454.1:n.1155-162_1155-158del
ENST00000464627.5:n.482-162_482-158del (FANCC)
ENST00000477942.5:n.510-162_510-158del (FANCC)
ENST00000480712.5:n.340-162_340-158del (FANCC)
ENST00000490972.6:c.1155-162_1155-158del (FANCC)	ENSP00000479931.1:n.1155-162_1155-158del
NM_000136.2:c.1155-162_1155-158del , LRG_497t1:c.1155-162_1155-158del (FANCC)	NP_000127.2:n.1155-162_1155-158del
NM_001243743.1:c.1155-162_1155-158del (FANCC)	NP_001230672.1:n.1155-162_1155-158del
NM_001243744.1:c.1155-162_1155-158del (FANCC)	NP_001230673.1:n.1155-162_1155-158del
XM_005251802.2:c.474-162_474-158del (FANCC)	XP_005251859.1:n.474-162_474-158del
XM_006717001.1:c.990-162_990-158del (FANCC)	XP_006717064.1:n.990-162_990-158del
XM_006717002.2:c.1155-162_1155-158del (FANCC)	XP_006717065.1:n.1155-162_1155-158del
XM_006717004.2:c.*50-162_*50-158del (FANCC)	XP_006717067.1:n.*50-162_*50-158del
XM_011518365.1:c.1155-162_1155-158del (FANCC)	XP_011516667.1:n.1155-162_1155-158del
XM_011518366.1:c.1155-162_1155-158del (FANCC)	XP_011516668.1:n.1155-162_1155-158del
XM_011518367.1:c.699-162_699-158del (FANCC)	XP_011516669.1:n.699-162_699-158del
XM_011519121.1:c.2319+31016_2319+31020del (AOPEP)	XP_011517423.1:n.2319+31016_2319+31020del
XM_005251802.3:c.474-162_474-158del (FANCC)	XP_005251859.1:n.474-162_474-158del
XM_006717001.3:c.990-162_990-158del (FANCC)	XP_006717064.1:n.990-162_990-158del
XM_006717002.4:c.1155-162_1155-158del (FANCC)	XP_006717065.1:n.1155-162_1155-158del
XM_006717004.4:c.*50-162_*50-158del (FANCC)	XP_006717067.1:n.*50-162_*50-158del
XM_011518365.3:c.1155-162_1155-158del (FANCC)	XP_011516667.1:n.1155-162_1155-158del
XM_011518366.3:c.1155-162_1155-158del (FANCC)	XP_011516668.1:n.1155-162_1155-158del
XM_011518367.2:c.699-162_699-158del (FANCC)	XP_011516669.1:n.699-162_699-158del
XM_011519121.3:c.2319+31016_2319+31020del (AOPEP)	XP_011517423.1:n.2319+31016_2319+31020del
XM_017014452.2:c.699-162_699-158del (FANCC)	XP_016869941.1:n.699-162_699-158del
XM_017014453.1:c.699-162_699-158del (FANCC)	XP_016869942.1:n.699-162_699-158del
XM_017014454.1:c.534-162_534-158del (FANCC)	XP_016869943.1:n.534-162_534-158del
XM_024447451.1:c.1155-162_1155-158del (FANCC)	XP_024303219.1:n.1155-162_1155-158del
NM_000136.3:c.1155-162_1155-158del (FANCC) MANE Select	NP_000127.2:n.1155-162_1155-158del
NM_001243743.2:c.1155-162_1155-158del (FANCC)	NP_001230672.1:n.1155-162_1155-158del
NM_001243744.2:c.1155-162_1155-158del (FANCC)	NP_001230673.1:n.1155-162_1155-158del