Canonical Allele Identifier: CA1865459528

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95101759C= , CM000671.2:g.95101759C=	GRCh38
NC_000009.11:g.97864041C= , CM000671.1:g.97864041C=	GRCh37
NC_000009.10:g.96903862C=	NCBI36
NG_011707.1:g.220951G= , LRG_497:g.220951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+20979C= (AOPEP)
ENST00000696260.1:n.2440G= (FANCC)
ENST00000289081.8:c.1625G= (FANCC) MANE Select	ENSP00000289081.3:p.Arg542=
ENST00000375305.6:c.1625G= (FANCC)	ENSP00000364454.1:p.Arg542=
ENST00000649334.1:c.1770G= (FANCC)	ENSP00000497735.1:n.1770G=
ENST00000289081.7:c.1625G= (FANCC)	ENSP00000289081.3:p.Arg542=
ENST00000375305.5:c.1625G= (FANCC)	ENSP00000364454.1:p.Arg542=
NM_000136.2:c.1625G= , LRG_497t1:c.1625G= (FANCC)	NP_000127.2:p.Arg542=
NM_001243743.1:c.1625G= (FANCC)	NP_001230672.1:p.Arg542=
XM_005251802.2:c.944G= (FANCC)	XP_005251859.1:p.Arg315=
XM_006717001.1:c.1460G= (FANCC)	XP_006717064.1:p.Arg487=
XM_011518365.1:c.1625G= (FANCC)	XP_011516667.1:p.Arg542=
XM_011518367.1:c.1169G= (FANCC)	XP_011516669.1:p.Arg390=
XM_011519121.1:c.2319+20979C= (AOPEP)	XP_011517423.1:n.2319+20979C=
XM_005251802.3:c.944G= (FANCC)	XP_005251859.1:p.Arg315=
XM_006717001.3:c.1460G= (FANCC)	XP_006717064.1:p.Arg487=
XM_011518365.3:c.1625G= (FANCC)	XP_011516667.1:p.Arg542=
XM_011518367.2:c.1169G= (FANCC)	XP_011516669.1:p.Arg390=
XM_011519121.3:c.2319+20979C= (AOPEP)	XP_011517423.1:n.2319+20979C=
XM_017014452.2:c.1169G= (FANCC)	XP_016869941.1:p.Arg390=
XM_017014453.1:c.1169G= (FANCC)	XP_016869942.1:p.Arg390=
XM_017014454.1:c.1004G= (FANCC)	XP_016869943.1:p.Arg335=
XM_024447451.1:c.1625G= (FANCC)	XP_024303219.1:p.Arg542=
NM_000136.3:c.1625G= (FANCC) MANE Select	NP_000127.2:p.Arg542=
NM_001243743.2:c.1625G= (FANCC)	NP_001230672.1:p.Arg542=