Canonical Allele Identifier: CA466092106

Gene: AOPEP FANCC

Linked Data

• ClinVar Variation Id: 3230368
• ClinVar RCV Id: RCV004520519
• MyVariant Identifiers: chr9:g.97864103C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95101821C>T , CM000671.2:g.95101821C>T	GRCh38
NC_000009.11:g.97864103C>T , CM000671.1:g.97864103C>T	GRCh37
NC_000009.10:g.96903924C>T	NCBI36
NG_011707.1:g.220889G>A , LRG_497:g.220889G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+21041C>T (AOPEP)
ENST00000696260.1:n.2378G>A (FANCC)
ENST00000289081.8:c.1563G>A (FANCC) MANE Select	ENSP00000289081.3:p.Glu521=
ENST00000375305.6:c.1563G>A (FANCC)	ENSP00000364454.1:p.Glu521=
ENST00000649334.1:c.1708G>A (FANCC)	ENSP00000497735.1:n.1708G>A
ENST00000289081.7:c.1563G>A (FANCC)	ENSP00000289081.3:p.Glu521=
ENST00000375305.5:c.1563G>A (FANCC)	ENSP00000364454.1:p.Glu521=
NM_000136.2:c.1563G>A , LRG_497t1:c.1563G>A (FANCC)	NP_000127.2:p.Glu521=
NM_001243743.1:c.1563G>A (FANCC)	NP_001230672.1:p.Glu521=
XM_005251802.2:c.882G>A (FANCC)	XP_005251859.1:p.Glu294=
XM_006717001.1:c.1398G>A (FANCC)	XP_006717064.1:p.Glu466=
XM_011518365.1:c.1563G>A (FANCC)	XP_011516667.1:p.Glu521=
XM_011518367.1:c.1107G>A (FANCC)	XP_011516669.1:p.Glu369=
XM_011519121.1:c.2319+21041C>T (AOPEP)	XP_011517423.1:n.2319+21041C>T
XM_005251802.3:c.882G>A (FANCC)	XP_005251859.1:p.Glu294=
XM_006717001.3:c.1398G>A (FANCC)	XP_006717064.1:p.Glu466=
XM_011518365.3:c.1563G>A (FANCC)	XP_011516667.1:p.Glu521=
XM_011518367.2:c.1107G>A (FANCC)	XP_011516669.1:p.Glu369=
XM_011519121.3:c.2319+21041C>T (AOPEP)	XP_011517423.1:n.2319+21041C>T
XM_017014452.2:c.1107G>A (FANCC)	XP_016869941.1:p.Glu369=
XM_017014453.1:c.1107G>A (FANCC)	XP_016869942.1:p.Glu369=
XM_017014454.1:c.942G>A (FANCC)	XP_016869943.1:p.Glu314=
XM_024447451.1:c.1563G>A (FANCC)	XP_024303219.1:p.Glu521=
NM_000136.3:c.1563G>A (FANCC) MANE Select	NP_000127.2:p.Glu521=
NM_001243743.2:c.1563G>A (FANCC)	NP_001230672.1:p.Glu521=