Canonical Allele Identifier: CA466092334

Gene: AOPEP FANCC

Linked Data

• dbSNP Id: rs2134455660
• MyVariant Identifiers: chr9:g.97869459G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107177G>C , CM000671.2:g.95107177G>C	GRCh38
NC_000009.11:g.97869459G>C , CM000671.1:g.97869459G>C	GRCh37
NC_000009.10:g.96909280G>C	NCBI36
NG_011707.1:g.215533C>G , LRG_497:g.215533C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000710812.1:n.410+26397G>C (AOPEP)
ENST00000696260.1:n.2237C>G (FANCC)
ENST00000289081.8:c.1422C>G (FANCC) MANE Select	ENSP00000289081.3:p.Gly474=
ENST00000375305.6:c.1422C>G (FANCC)	ENSP00000364454.1:p.Gly474=
ENST00000649334.1:c.1567C>G (FANCC)	ENSP00000497735.1:n.1567C>G
ENST00000289081.7:c.1422C>G (FANCC)	ENSP00000289081.3:p.Gly474=
ENST00000375305.5:c.1422C>G (FANCC)	ENSP00000364454.1:p.Gly474=
ENST00000464627.5:n.749C>G (FANCC)
NM_000136.2:c.1422C>G , LRG_497t1:c.1422C>G (FANCC)	NP_000127.2:p.Gly474=
NM_001243743.1:c.1422C>G (FANCC)	NP_001230672.1:p.Gly474=
XM_005251802.2:c.741C>G (FANCC)	XP_005251859.1:p.Gly247=
XM_006717001.1:c.1257C>G (FANCC)	XP_006717064.1:p.Gly419=
XM_011518365.1:c.1422C>G (FANCC)	XP_011516667.1:p.Gly474=
XM_011518367.1:c.966C>G (FANCC)	XP_011516669.1:p.Gly322=
XM_011519121.1:c.2319+26397G>C (AOPEP)	XP_011517423.1:n.2319+26397G>C
XM_005251802.3:c.741C>G (FANCC)	XP_005251859.1:p.Gly247=
XM_006717001.3:c.1257C>G (FANCC)	XP_006717064.1:p.Gly419=
XM_011518365.3:c.1422C>G (FANCC)	XP_011516667.1:p.Gly474=
XM_011518367.2:c.966C>G (FANCC)	XP_011516669.1:p.Gly322=
XM_011519121.3:c.2319+26397G>C (AOPEP)	XP_011517423.1:n.2319+26397G>C
XM_017014452.2:c.966C>G (FANCC)	XP_016869941.1:p.Gly322=
XM_017014453.1:c.966C>G (FANCC)	XP_016869942.1:p.Gly322=
XM_017014454.1:c.801C>G (FANCC)	XP_016869943.1:p.Gly267=
XM_024447451.1:c.1422C>G (FANCC)	XP_024303219.1:p.Gly474=
XR_001746847.1:n.595G>C
NM_000136.3:c.1422C>G (FANCC) MANE Select	NP_000127.2:p.Gly474=
NM_001243743.2:c.1422C>G (FANCC)	NP_001230672.1:p.Gly474=