Canonical Allele Identifier: CA466092331

Gene: AOPEP FANCC

Linked Data

• MyVariant Identifiers: chr9:g.97869456T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107174T>G , CM000671.2:g.95107174T>G	GRCh38
NC_000009.11:g.97869456T>G , CM000671.1:g.97869456T>G	GRCh37
NC_000009.10:g.96909277T>G	NCBI36
NG_011707.1:g.215536A>C , LRG_497:g.215536A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000710812.1:n.410+26394T>G (AOPEP)
ENST00000696260.1:n.2240A>C (FANCC)
ENST00000289081.8:c.1425A>C (FANCC) MANE Select	ENSP00000289081.3:p.Thr475=
ENST00000375305.6:c.1425A>C (FANCC)	ENSP00000364454.1:p.Thr475=
ENST00000649334.1:c.1570A>C (FANCC)	ENSP00000497735.1:n.1570A>C
ENST00000289081.7:c.1425A>C (FANCC)	ENSP00000289081.3:p.Thr475=
ENST00000375305.5:c.1425A>C (FANCC)	ENSP00000364454.1:p.Thr475=
ENST00000464627.5:n.752A>C (FANCC)
NM_000136.2:c.1425A>C , LRG_497t1:c.1425A>C (FANCC)	NP_000127.2:p.Thr475=
NM_001243743.1:c.1425A>C (FANCC)	NP_001230672.1:p.Thr475=
XM_005251802.2:c.744A>C (FANCC)	XP_005251859.1:p.Thr248=
XM_006717001.1:c.1260A>C (FANCC)	XP_006717064.1:p.Thr420=
XM_011518365.1:c.1425A>C (FANCC)	XP_011516667.1:p.Thr475=
XM_011518367.1:c.969A>C (FANCC)	XP_011516669.1:p.Thr323=
XM_011519121.1:c.2319+26394T>G (AOPEP)	XP_011517423.1:n.2319+26394T>G
XM_005251802.3:c.744A>C (FANCC)	XP_005251859.1:p.Thr248=
XM_006717001.3:c.1260A>C (FANCC)	XP_006717064.1:p.Thr420=
XM_011518365.3:c.1425A>C (FANCC)	XP_011516667.1:p.Thr475=
XM_011518367.2:c.969A>C (FANCC)	XP_011516669.1:p.Thr323=
XM_011519121.3:c.2319+26394T>G (AOPEP)	XP_011517423.1:n.2319+26394T>G
XM_017014452.2:c.969A>C (FANCC)	XP_016869941.1:p.Thr323=
XM_017014453.1:c.969A>C (FANCC)	XP_016869942.1:p.Thr323=
XM_017014454.1:c.804A>C (FANCC)	XP_016869943.1:p.Thr268=
XM_024447451.1:c.1425A>C (FANCC)	XP_024303219.1:p.Thr475=
XR_001746847.1:n.592T>G
NM_000136.3:c.1425A>C (FANCC) MANE Select	NP_000127.2:p.Thr475=
NM_001243743.2:c.1425A>C (FANCC)	NP_001230672.1:p.Thr475=