Canonical Allele Identifier: CA589258034

Gene: AOPEP FANCC

Linked Data

• dbSNP Id: rs1218612491
• gnomAD v2: 9-97864165-AAC-A
• gnomAD v4: 9-95101883-AAC-A
• MyVariant Identifiers: chr9:g.97864166_97864167del (hg19) ; chr9:g.95101884_95101885del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95101886_95101887del , CM000671.2:g.95101886_95101887del	GRCh38
NC_000009.11:g.97864168_97864169del , CM000671.1:g.97864168_97864169del	GRCh37
NC_000009.10:g.96903989_96903990del	NCBI36
NG_011707.1:g.220825_220826del , LRG_497:g.220825_220826del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+21106_410+21107del (AOPEP)
ENST00000696260.1:n.2349-35_2349-34del (FANCC)
ENST00000289081.8:c.1534-35_1534-34del (FANCC) MANE Select	ENSP00000289081.3:n.1534-35_1534-34del
ENST00000375305.6:c.1534-35_1534-34del (FANCC)	ENSP00000364454.1:n.1534-35_1534-34del
ENST00000649334.1:c.1679-35_1679-34del (FANCC)	ENSP00000497735.1:n.1679-35_1679-34del
ENST00000289081.7:c.1534-35_1534-34del (FANCC)	ENSP00000289081.3:n.1534-35_1534-34del
ENST00000375305.5:c.1534-35_1534-34del (FANCC)	ENSP00000364454.1:n.1534-35_1534-34del
NM_000136.2:c.1534-35_1534-34del , LRG_497t1:c.1534-35_1534-34del (FANCC)	NP_000127.2:n.1534-35_1534-34del
NM_001243743.1:c.1534-35_1534-34del (FANCC)	NP_001230672.1:n.1534-35_1534-34del
XM_005251802.2:c.853-35_853-34del (FANCC)	XP_005251859.1:n.853-35_853-34del
XM_006717001.1:c.1369-35_1369-34del (FANCC)	XP_006717064.1:n.1369-35_1369-34del
XM_011518365.1:c.1534-35_1534-34del (FANCC)	XP_011516667.1:n.1534-35_1534-34del
XM_011518367.1:c.1078-35_1078-34del (FANCC)	XP_011516669.1:n.1078-35_1078-34del
XM_011519121.1:c.2319+21106_2319+21107del (AOPEP)	XP_011517423.1:n.2319+21106_2319+21107del
XM_005251802.3:c.853-35_853-34del (FANCC)	XP_005251859.1:n.853-35_853-34del
XM_006717001.3:c.1369-35_1369-34del (FANCC)	XP_006717064.1:n.1369-35_1369-34del
XM_011518365.3:c.1534-35_1534-34del (FANCC)	XP_011516667.1:n.1534-35_1534-34del
XM_011518367.2:c.1078-35_1078-34del (FANCC)	XP_011516669.1:n.1078-35_1078-34del
XM_011519121.3:c.2319+21106_2319+21107del (AOPEP)	XP_011517423.1:n.2319+21106_2319+21107del
XM_017014452.2:c.1078-35_1078-34del (FANCC)	XP_016869941.1:n.1078-35_1078-34del
XM_017014453.1:c.1078-35_1078-34del (FANCC)	XP_016869942.1:n.1078-35_1078-34del
XM_017014454.1:c.913-35_913-34del (FANCC)	XP_016869943.1:n.913-35_913-34del
XM_024447451.1:c.1534-35_1534-34del (FANCC)	XP_024303219.1:n.1534-35_1534-34del
NM_000136.3:c.1534-35_1534-34del (FANCC) MANE Select	NP_000127.2:n.1534-35_1534-34del
NM_001243743.2:c.1534-35_1534-34del (FANCC)	NP_001230672.1:n.1534-35_1534-34del