Canonical Allele Identifier: CA1865464157

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95111328_95111329delinsTG , CM000671.2:g.95111328_95111329delinsTG	GRCh38
NC_000009.11:g.97873610_97873611delinsTG , CM000671.1:g.97873610_97873611delinsTG	GRCh37
NC_000009.10:g.96913431_96913432delinsTG	NCBI36
NG_011707.1:g.211381_211382delinsCA , LRG_497:g.211381_211382delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+30548_410+30549delinsTG (AOPEP)
ENST00000696260.1:n.2144+134_2144+135delinsCA (FANCC)
ENST00000289081.8:c.1329+134_1329+135delinsCA (FANCC) MANE Select	ENSP00000289081.3:n.1329+134_1329+135delinsCA
ENST00000375305.6:c.1329+134_1329+135delinsCA (FANCC)	ENSP00000364454.1:n.1329+134_1329+135delinsCA
ENST00000490972.7:c.1346_1347delinsCA (FANCC)	ENSP00000479931.1:p.Ala449=
ENST00000649334.1:c.1474+134_1474+135delinsCA (FANCC)	ENSP00000497735.1:n.1474+134_1474+135delinsCA
ENST00000289081.7:c.1329+134_1329+135delinsCA (FANCC)	ENSP00000289081.3:n.1329+134_1329+135delinsCA
ENST00000375305.5:c.1329+134_1329+135delinsCA (FANCC)	ENSP00000364454.1:n.1329+134_1329+135delinsCA
ENST00000464627.5:n.656+134_656+135delinsCA (FANCC)
ENST00000477942.5:n.684+134_684+135delinsCA (FANCC)
ENST00000480712.5:n.514+134_514+135delinsCA (FANCC)
ENST00000490972.6:c.1346_1347delinsCA (FANCC)	ENSP00000479931.1:p.Ala449=
NM_000136.2:c.1329+134_1329+135delinsCA , LRG_497t1:c.1329+134_1329+135delinsCA (FANCC)	NP_000127.2:n.1329+134_1329+135delinsCA
NM_001243743.1:c.1329+134_1329+135delinsCA (FANCC)	NP_001230672.1:n.1329+134_1329+135delinsCA
NM_001243744.1:c.1346_1347delinsCA (FANCC)	NP_001230673.1:p.Ala449=
XM_005251802.2:c.648+134_648+135delinsCA (FANCC)	XP_005251859.1:n.648+134_648+135delinsCA
XM_006717001.1:c.1164+134_1164+135delinsCA (FANCC)	XP_006717064.1:n.1164+134_1164+135delinsCA
XM_006717002.2:c.1329+134_1329+135delinsCA (FANCC)	XP_006717065.1:n.1329+134_1329+135delinsCA
XM_011518365.1:c.1329+134_1329+135delinsCA (FANCC)	XP_011516667.1:n.1329+134_1329+135delinsCA
XM_011518366.1:c.1330-10_1330-9delinsCA (FANCC)	XP_011516668.1:n.1330-10_1330-9delinsCA
XM_011518367.1:c.873+134_873+135delinsCA (FANCC)	XP_011516669.1:n.873+134_873+135delinsCA
XM_011519121.1:c.2319+30548_2319+30549delinsTG (AOPEP)	XP_011517423.1:n.2319+30548_2319+30549delinsTG
XM_005251802.3:c.648+134_648+135delinsCA (FANCC)	XP_005251859.1:n.648+134_648+135delinsCA
XM_006717001.3:c.1164+134_1164+135delinsCA (FANCC)	XP_006717064.1:n.1164+134_1164+135delinsCA
XM_006717002.4:c.1329+134_1329+135delinsCA (FANCC)	XP_006717065.1:n.1329+134_1329+135delinsCA
XM_011518365.3:c.1329+134_1329+135delinsCA (FANCC)	XP_011516667.1:n.1329+134_1329+135delinsCA
XM_011518366.3:c.1330-10_1330-9delinsCA (FANCC)	XP_011516668.1:n.1330-10_1330-9delinsCA
XM_011518367.2:c.873+134_873+135delinsCA (FANCC)	XP_011516669.1:n.873+134_873+135delinsCA
XM_011519121.3:c.2319+30548_2319+30549delinsTG (AOPEP)	XP_011517423.1:n.2319+30548_2319+30549delinsTG
XM_017014452.2:c.873+134_873+135delinsCA (FANCC)	XP_016869941.1:n.873+134_873+135delinsCA
XM_017014453.1:c.873+134_873+135delinsCA (FANCC)	XP_016869942.1:n.873+134_873+135delinsCA
XM_017014454.1:c.708+134_708+135delinsCA (FANCC)	XP_016869943.1:n.708+134_708+135delinsCA
XM_024447451.1:c.1329+134_1329+135delinsCA (FANCC)	XP_024303219.1:n.1329+134_1329+135delinsCA
NM_000136.3:c.1329+134_1329+135delinsCA (FANCC) MANE Select	NP_000127.2:n.1329+134_1329+135delinsCA
NM_001243743.2:c.1329+134_1329+135delinsCA (FANCC)	NP_001230672.1:n.1329+134_1329+135delinsCA
NM_001243744.2:c.1346_1347delinsCA (FANCC)	NP_001230673.1:p.Ala449=