Canonical Allele Identifier: CA2843647059

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95101667T>C , CM000671.2:g.95101667T>C	GRCh38
NC_000009.11:g.97863949T>C , CM000671.1:g.97863949T>C	GRCh37
NC_000009.10:g.96903770T>C	NCBI36
NG_011707.1:g.221043A>G , LRG_497:g.221043A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+20887T>C (AOPEP)
ENST00000696260.1:n.2532A>G (FANCC)
ENST00000289081.8:c.*40A>G (FANCC) MANE Select	ENSP00000289081.3:n.*40A>G
ENST00000375305.6:c.*40A>G (FANCC)	ENSP00000364454.1:n.*40A>G
ENST00000289081.7:c.*40A>G (FANCC)	ENSP00000289081.3:n.*40A>G
ENST00000375305.5:c.*40A>G (FANCC)	ENSP00000364454.1:n.*40A>G
NM_000136.2:c.*40A>G , LRG_497t1:c.*40A>G (FANCC)	NP_000127.2:n.*40A>G
NM_001243743.1:c.*40A>G (FANCC)	NP_001230672.1:n.*40A>G
XM_005251802.2:c.*40A>G (FANCC)	XP_005251859.1:n.*40A>G
XM_006717001.1:c.*40A>G (FANCC)	XP_006717064.1:n.*40A>G
XM_011518365.1:c.*40A>G (FANCC)	XP_011516667.1:n.*40A>G
XM_011518367.1:c.*40A>G (FANCC)	XP_011516669.1:n.*40A>G
XM_011519121.1:c.2319+20887T>C (AOPEP)	XP_011517423.1:n.2319+20887T>C
XM_005251802.3:c.*40A>G (FANCC)	XP_005251859.1:n.*40A>G
XM_006717001.3:c.*40A>G (FANCC)	XP_006717064.1:n.*40A>G
XM_011518365.3:c.*40A>G (FANCC)	XP_011516667.1:n.*40A>G
XM_011518367.2:c.*40A>G (FANCC)	XP_011516669.1:n.*40A>G
XM_011519121.3:c.2319+20887T>C (AOPEP)	XP_011517423.1:n.2319+20887T>C
XM_017014452.2:c.*40A>G (FANCC)	XP_016869941.1:n.*40A>G
XM_017014453.1:c.*40A>G (FANCC)	XP_016869942.1:n.*40A>G
XM_017014454.1:c.*40A>G (FANCC)	XP_016869943.1:n.*40A>G
XM_024447451.1:c.*40A>G (FANCC)	XP_024303219.1:n.*40A>G
NM_000136.3:c.*40A>G (FANCC) MANE Select	NP_000127.2:n.*40A>G
NM_001243743.2:c.*40A>G (FANCC)	NP_001230672.1:n.*40A>G