Canonical Allele Identifier: CA1865462284

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107381_95107383delinsCCT , CM000671.2:g.95107381_95107383delinsCCT	GRCh38
NC_000009.11:g.97869663_97869665delinsCCT , CM000671.1:g.97869663_97869665delinsCCT	GRCh37
NC_000009.10:g.96909484_96909486delinsCCT	NCBI36
NG_011707.1:g.215327_215329delinsAGG , LRG_497:g.215327_215329delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+26601_410+26603delinsCCT (AOPEP)
ENST00000696260.1:n.2145-114_2145-112delinsAGG (FANCC)
ENST00000289081.8:c.1330-114_1330-112delinsAGG (FANCC) MANE Select	ENSP00000289081.3:n.1330-114_1330-112delinsAGG
ENST00000375305.6:c.1330-114_1330-112delinsAGG (FANCC)	ENSP00000364454.1:n.1330-114_1330-112delinsAGG
ENST00000649334.1:c.1475-114_1475-112delinsAGG (FANCC)	ENSP00000497735.1:n.1475-114_1475-112delinsAGG
ENST00000289081.7:c.1330-114_1330-112delinsAGG (FANCC)	ENSP00000289081.3:n.1330-114_1330-112delinsAGG
ENST00000375305.5:c.1330-114_1330-112delinsAGG (FANCC)	ENSP00000364454.1:n.1330-114_1330-112delinsAGG
ENST00000464627.5:n.657-114_657-112delinsAGG (FANCC)
ENST00000480712.5:n.645_647delinsAGG (FANCC)
NM_000136.2:c.1330-114_1330-112delinsAGG , LRG_497t1:c.1330-114_1330-112delinsAGG (FANCC)	NP_000127.2:n.1330-114_1330-112delinsAGG
NM_001243743.1:c.1330-114_1330-112delinsAGG (FANCC)	NP_001230672.1:n.1330-114_1330-112delinsAGG
XM_005251802.2:c.649-114_649-112delinsAGG (FANCC)	XP_005251859.1:n.649-114_649-112delinsAGG
XM_006717001.1:c.1165-114_1165-112delinsAGG (FANCC)	XP_006717064.1:n.1165-114_1165-112delinsAGG
XM_006717002.2:c.*95_*97delinsAGG (FANCC)	XP_006717065.1:n.*95_*97delinsAGG
XM_011518365.1:c.1330-114_1330-112delinsAGG (FANCC)	XP_011516667.1:n.1330-114_1330-112delinsAGG
XM_011518367.1:c.874-114_874-112delinsAGG (FANCC)	XP_011516669.1:n.874-114_874-112delinsAGG
XM_011519121.1:c.2319+26601_2319+26603delinsCCT (AOPEP)	XP_011517423.1:n.2319+26601_2319+26603delinsCCT
XM_005251802.3:c.649-114_649-112delinsAGG (FANCC)	XP_005251859.1:n.649-114_649-112delinsAGG
XM_006717001.3:c.1165-114_1165-112delinsAGG (FANCC)	XP_006717064.1:n.1165-114_1165-112delinsAGG
XM_006717002.4:c.*95_*97delinsAGG (FANCC)	XP_006717065.1:n.*95_*97delinsAGG
XM_011518365.3:c.1330-114_1330-112delinsAGG (FANCC)	XP_011516667.1:n.1330-114_1330-112delinsAGG
XM_011518367.2:c.874-114_874-112delinsAGG (FANCC)	XP_011516669.1:n.874-114_874-112delinsAGG
XM_011519121.3:c.2319+26601_2319+26603delinsCCT (AOPEP)	XP_011517423.1:n.2319+26601_2319+26603delinsCCT
XM_017014452.2:c.874-114_874-112delinsAGG (FANCC)	XP_016869941.1:n.874-114_874-112delinsAGG
XM_017014453.1:c.874-114_874-112delinsAGG (FANCC)	XP_016869942.1:n.874-114_874-112delinsAGG
XM_017014454.1:c.709-114_709-112delinsAGG (FANCC)	XP_016869943.1:n.709-114_709-112delinsAGG
XM_024447451.1:c.1330-114_1330-112delinsAGG (FANCC)	XP_024303219.1:n.1330-114_1330-112delinsAGG
XR_001746847.1:n.799_801delinsCCT
NM_000136.3:c.1330-114_1330-112delinsAGG (FANCC) MANE Select	NP_000127.2:n.1330-114_1330-112delinsAGG
NM_001243743.2:c.1330-114_1330-112delinsAGG (FANCC)	NP_001230672.1:n.1330-114_1330-112delinsAGG