Canonical Allele Identifier: CA589259669

Gene: AOPEP FANCC

Linked Data

• gnomAD v2: 9-97874200-A-AC
• MyVariant Identifiers: chr9:g.97874200_97874201insC (hg19) ; chr9:g.95111918_95111919insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95111918_95111919insC , CM000671.2:g.95111918_95111919insC	GRCh38
NC_000009.11:g.97874200_97874201insC , CM000671.1:g.97874200_97874201insC	GRCh37
NC_000009.10:g.96914021_96914022insC	NCBI36
NG_011707.1:g.210791_210792insG , LRG_497:g.210791_210792insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+31138_410+31139insC (AOPEP)
ENST00000696260.1:n.1688_1689insG (FANCC)
ENST00000289081.8:c.1155-282_1155-281insG (FANCC) MANE Select	ENSP00000289081.3:n.1155-282_1155-281insG
ENST00000375305.6:c.1155-282_1155-281insG (FANCC)	ENSP00000364454.1:n.1155-282_1155-281insG
ENST00000490972.7:c.1155-282_1155-281insG (FANCC)	ENSP00000479931.1:n.1155-282_1155-281insG
ENST00000649334.1:c.1300-282_1300-281insG (FANCC)	ENSP00000497735.1:n.1300-282_1300-281insG
ENST00000289081.7:c.1155-282_1155-281insG (FANCC)	ENSP00000289081.3:n.1155-282_1155-281insG
ENST00000375305.5:c.1155-282_1155-281insG (FANCC)	ENSP00000364454.1:n.1155-282_1155-281insG
ENST00000464627.5:n.482-282_482-281insG (FANCC)
ENST00000477942.5:n.510-282_510-281insG (FANCC)
ENST00000480712.5:n.340-282_340-281insG (FANCC)
ENST00000490972.6:c.1155-282_1155-281insG (FANCC)	ENSP00000479931.1:n.1155-282_1155-281insG
NM_000136.2:c.1155-282_1155-281insG , LRG_497t1:c.1155-282_1155-281insG (FANCC)	NP_000127.2:n.1155-282_1155-281insG
NM_001243743.1:c.1155-282_1155-281insG (FANCC)	NP_001230672.1:n.1155-282_1155-281insG
NM_001243744.1:c.1155-282_1155-281insG (FANCC)	NP_001230673.1:n.1155-282_1155-281insG
XM_005251802.2:c.474-282_474-281insG (FANCC)	XP_005251859.1:n.474-282_474-281insG
XM_006717001.1:c.990-282_990-281insG (FANCC)	XP_006717064.1:n.990-282_990-281insG
XM_006717002.2:c.1155-282_1155-281insG (FANCC)	XP_006717065.1:n.1155-282_1155-281insG
XM_006717004.2:c.*50-282_*50-281insG (FANCC)	XP_006717067.1:n.*50-282_*50-281insG
XM_011518365.1:c.1155-282_1155-281insG (FANCC)	XP_011516667.1:n.1155-282_1155-281insG
XM_011518366.1:c.1155-282_1155-281insG (FANCC)	XP_011516668.1:n.1155-282_1155-281insG
XM_011518367.1:c.699-282_699-281insG (FANCC)	XP_011516669.1:n.699-282_699-281insG
XM_011519121.1:c.2319+31138_2319+31139insC (AOPEP)	XP_011517423.1:n.2319+31138_2319+31139insC
XM_005251802.3:c.474-282_474-281insG (FANCC)	XP_005251859.1:n.474-282_474-281insG
XM_006717001.3:c.990-282_990-281insG (FANCC)	XP_006717064.1:n.990-282_990-281insG
XM_006717002.4:c.1155-282_1155-281insG (FANCC)	XP_006717065.1:n.1155-282_1155-281insG
XM_006717004.4:c.*50-282_*50-281insG (FANCC)	XP_006717067.1:n.*50-282_*50-281insG
XM_011518365.3:c.1155-282_1155-281insG (FANCC)	XP_011516667.1:n.1155-282_1155-281insG
XM_011518366.3:c.1155-282_1155-281insG (FANCC)	XP_011516668.1:n.1155-282_1155-281insG
XM_011518367.2:c.699-282_699-281insG (FANCC)	XP_011516669.1:n.699-282_699-281insG
XM_011519121.3:c.2319+31138_2319+31139insC (AOPEP)	XP_011517423.1:n.2319+31138_2319+31139insC
XM_017014452.2:c.699-282_699-281insG (FANCC)	XP_016869941.1:n.699-282_699-281insG
XM_017014453.1:c.699-282_699-281insG (FANCC)	XP_016869942.1:n.699-282_699-281insG
XM_017014454.1:c.534-282_534-281insG (FANCC)	XP_016869943.1:n.534-282_534-281insG
XM_024447451.1:c.1155-282_1155-281insG (FANCC)	XP_024303219.1:n.1155-282_1155-281insG
NM_000136.3:c.1155-282_1155-281insG (FANCC) MANE Select	NP_000127.2:n.1155-282_1155-281insG
NM_001243743.2:c.1155-282_1155-281insG (FANCC)	NP_001230672.1:n.1155-282_1155-281insG
NM_001243744.2:c.1155-282_1155-281insG (FANCC)	NP_001230673.1:n.1155-282_1155-281insG