Canonical Allele Identifier: CA1865459556

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95101797G= , CM000671.2:g.95101797G=	GRCh38
NC_000009.11:g.97864079G= , CM000671.1:g.97864079G=	GRCh37
NC_000009.10:g.96903900G=	NCBI36
NG_011707.1:g.220913C= , LRG_497:g.220913C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+21017G= (AOPEP)
ENST00000696260.1:n.2402C= (FANCC)
ENST00000289081.8:c.1587C= (FANCC) MANE Select	ENSP00000289081.3:p.Thr529=
ENST00000375305.6:c.1587C= (FANCC)	ENSP00000364454.1:p.Thr529=
ENST00000649334.1:c.1732C= (FANCC)	ENSP00000497735.1:n.1732C=
ENST00000289081.7:c.1587C= (FANCC)	ENSP00000289081.3:p.Thr529=
ENST00000375305.5:c.1587C= (FANCC)	ENSP00000364454.1:p.Thr529=
NM_000136.2:c.1587C= , LRG_497t1:c.1587C= (FANCC)	NP_000127.2:p.Thr529=
NM_001243743.1:c.1587C= (FANCC)	NP_001230672.1:p.Thr529=
XM_005251802.2:c.906C= (FANCC)	XP_005251859.1:p.Thr302=
XM_006717001.1:c.1422C= (FANCC)	XP_006717064.1:p.Thr474=
XM_011518365.1:c.1587C= (FANCC)	XP_011516667.1:p.Thr529=
XM_011518367.1:c.1131C= (FANCC)	XP_011516669.1:p.Thr377=
XM_011519121.1:c.2319+21017G= (AOPEP)	XP_011517423.1:n.2319+21017G=
XM_005251802.3:c.906C= (FANCC)	XP_005251859.1:p.Thr302=
XM_006717001.3:c.1422C= (FANCC)	XP_006717064.1:p.Thr474=
XM_011518365.3:c.1587C= (FANCC)	XP_011516667.1:p.Thr529=
XM_011518367.2:c.1131C= (FANCC)	XP_011516669.1:p.Thr377=
XM_011519121.3:c.2319+21017G= (AOPEP)	XP_011517423.1:n.2319+21017G=
XM_017014452.2:c.1131C= (FANCC)	XP_016869941.1:p.Thr377=
XM_017014453.1:c.1131C= (FANCC)	XP_016869942.1:p.Thr377=
XM_017014454.1:c.966C= (FANCC)	XP_016869943.1:p.Thr322=
XM_024447451.1:c.1587C= (FANCC)	XP_024303219.1:p.Thr529=
NM_000136.3:c.1587C= (FANCC) MANE Select	NP_000127.2:p.Thr529=
NM_001243743.2:c.1587C= (FANCC)	NP_001230672.1:p.Thr529=