Canonical Allele Identifier: CA1865462198

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107241_95107244delinsAGGT , CM000671.2:g.95107241_95107244delinsAGGT	GRCh38
NC_000009.11:g.97869523_97869526delinsAGGT , CM000671.1:g.97869523_97869526delinsAGGT	GRCh37
NC_000009.10:g.96909344_96909347delinsAGGT	NCBI36
NG_011707.1:g.215466_215469delinsACCT , LRG_497:g.215466_215469delinsACCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000710812.1:n.410+26461_410+26464delinsAGGT (AOPEP)
ENST00000696260.1:n.2170_2173delinsACCT (FANCC)
ENST00000289081.8:c.1355_1358delinsACCT (FANCC) MANE Select	ENSP00000289081.3:p.His452=
ENST00000375305.6:c.1355_1358delinsACCT (FANCC)	ENSP00000364454.1:p.His452=
ENST00000649334.1:c.1500_1503delinsACCT (FANCC)	ENSP00000497735.1:n.1500_1503delinsACCT
ENST00000289081.7:c.1355_1358delinsACCT (FANCC)	ENSP00000289081.3:p.His452=
ENST00000375305.5:c.1355_1358delinsACCT (FANCC)	ENSP00000364454.1:p.His452=
ENST00000464627.5:n.682_685delinsACCT (FANCC)
NM_000136.2:c.1355_1358delinsACCT , LRG_497t1:c.1355_1358delinsACCT (FANCC)	NP_000127.2:p.His452=
NM_001243743.1:c.1355_1358delinsACCT (FANCC)	NP_001230672.1:p.His452=
XM_005251802.2:c.674_677delinsACCT (FANCC)	XP_005251859.1:p.His225=
XM_006717001.1:c.1190_1193delinsACCT (FANCC)	XP_006717064.1:p.His397=
XM_011518365.1:c.1355_1358delinsACCT (FANCC)	XP_011516667.1:p.His452=
XM_011518367.1:c.899_902delinsACCT (FANCC)	XP_011516669.1:p.His300=
XM_011519121.1:c.2319+26461_2319+26464delinsAGGT (AOPEP)	XP_011517423.1:n.2319+26461_2319+26464delinsAGGT
XM_005251802.3:c.674_677delinsACCT (FANCC)	XP_005251859.1:p.His225=
XM_006717001.3:c.1190_1193delinsACCT (FANCC)	XP_006717064.1:p.His397=
XM_011518365.3:c.1355_1358delinsACCT (FANCC)	XP_011516667.1:p.His452=
XM_011518367.2:c.899_902delinsACCT (FANCC)	XP_011516669.1:p.His300=
XM_011519121.3:c.2319+26461_2319+26464delinsAGGT (AOPEP)	XP_011517423.1:n.2319+26461_2319+26464delinsAGGT
XM_017014452.2:c.899_902delinsACCT (FANCC)	XP_016869941.1:p.His300=
XM_017014453.1:c.899_902delinsACCT (FANCC)	XP_016869942.1:p.His300=
XM_017014454.1:c.734_737delinsACCT (FANCC)	XP_016869943.1:p.His245=
XM_024447451.1:c.1355_1358delinsACCT (FANCC)	XP_024303219.1:p.His452=
XR_001746847.1:n.659_662delinsAGGT
NM_000136.3:c.1355_1358delinsACCT (FANCC) MANE Select	NP_000127.2:p.His452=
NM_001243743.2:c.1355_1358delinsACCT (FANCC)	NP_001230672.1:p.His452=