Canonical Allele Identifier: CA589580899

Gene: AOPEP FANCC

Linked Data

• dbSNP Id: rs1360176396
• gnomAD v2: 9-97869584-G-C
• MyVariant Identifiers: chr9:g.97869584G>C (hg19) ; chr9:g.95107302G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107302G>C , CM000671.2:g.95107302G>C	GRCh38
NC_000009.11:g.97869584G>C , CM000671.1:g.97869584G>C	GRCh37
NC_000009.10:g.96909405G>C	NCBI36
NG_011707.1:g.215408C>G , LRG_497:g.215408C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+26522G>C (AOPEP)
ENST00000696260.1:n.2145-33C>G (FANCC)
ENST00000289081.8:c.1330-33C>G (FANCC) MANE Select	ENSP00000289081.3:n.1330-33C>G
ENST00000375305.6:c.1330-33C>G (FANCC)	ENSP00000364454.1:n.1330-33C>G
ENST00000649334.1:c.1475-33C>G (FANCC)	ENSP00000497735.1:n.1475-33C>G
ENST00000289081.7:c.1330-33C>G (FANCC)	ENSP00000289081.3:n.1330-33C>G
ENST00000375305.5:c.1330-33C>G (FANCC)	ENSP00000364454.1:n.1330-33C>G
ENST00000464627.5:n.657-33C>G (FANCC)
NM_000136.2:c.1330-33C>G , LRG_497t1:c.1330-33C>G (FANCC)	NP_000127.2:n.1330-33C>G
NM_001243743.1:c.1330-33C>G (FANCC)	NP_001230672.1:n.1330-33C>G
XM_005251802.2:c.649-33C>G (FANCC)	XP_005251859.1:n.649-33C>G
XM_006717001.1:c.1165-33C>G (FANCC)	XP_006717064.1:n.1165-33C>G
XM_011518365.1:c.1330-33C>G (FANCC)	XP_011516667.1:n.1330-33C>G
XM_011518367.1:c.874-33C>G (FANCC)	XP_011516669.1:n.874-33C>G
XM_011519121.1:c.2319+26522G>C (AOPEP)	XP_011517423.1:n.2319+26522G>C
XM_005251802.3:c.649-33C>G (FANCC)	XP_005251859.1:n.649-33C>G
XM_006717001.3:c.1165-33C>G (FANCC)	XP_006717064.1:n.1165-33C>G
XM_011518365.3:c.1330-33C>G (FANCC)	XP_011516667.1:n.1330-33C>G
XM_011518367.2:c.874-33C>G (FANCC)	XP_011516669.1:n.874-33C>G
XM_011519121.3:c.2319+26522G>C (AOPEP)	XP_011517423.1:n.2319+26522G>C
XM_017014452.2:c.874-33C>G (FANCC)	XP_016869941.1:n.874-33C>G
XM_017014453.1:c.874-33C>G (FANCC)	XP_016869942.1:n.874-33C>G
XM_017014454.1:c.709-33C>G (FANCC)	XP_016869943.1:n.709-33C>G
XM_024447451.1:c.1330-33C>G (FANCC)	XP_024303219.1:n.1330-33C>G
XR_001746847.1:n.720G>C
NM_000136.3:c.1330-33C>G (FANCC) MANE Select	NP_000127.2:n.1330-33C>G
NM_001243743.2:c.1330-33C>G (FANCC)	NP_001230672.1:n.1330-33C>G