Canonical Allele Identifier: CA2690792141

Gene: FANCC

Linked Data

• gnomAD v4: 9-95171282-A-ACATG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171282_95171283insCATG , CM000671.2:g.95171282_95171283insCATG	GRCh38
NC_000009.11:g.97933564_97933565insCATG , CM000671.1:g.97933564_97933565insCATG	GRCh37
NC_000009.10:g.96973385_96973386insCATG	NCBI36
NG_011707.1:g.151427_151428insCATG , LRG_497:g.151427_151428insCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.848-140_848-139insCATG
ENST00000289081.8:c.457-140_457-139insCATG MANE Select	ENSP00000289081.3:n.457-140_457-139insCATG
ENST00000375305.6:c.457-140_457-139insCATG	ENSP00000364454.1:n.457-140_457-139insCATG
ENST00000490972.7:c.457-140_457-139insCATG	ENSP00000479931.1:n.457-140_457-139insCATG
ENST00000636777.1:n.515-140_515-139insCATG
ENST00000647778.1:c.457-140_457-139insCATG	ENSP00000498125.1:n.457-140_457-139insCATG
ENST00000649334.1:c.602-140_602-139insCATG	ENSP00000497735.1:n.602-140_602-139insCATG
ENST00000649701.1:n.172-140_172-139insCATG
ENST00000289081.7:c.457-140_457-139insCATG	ENSP00000289081.3:n.457-140_457-139insCATG
ENST00000375305.5:c.457-140_457-139insCATG	ENSP00000364454.1:n.457-140_457-139insCATG
ENST00000474949.1:n.814-140_814-139insCATG
ENST00000490972.6:c.457-140_457-139insCATG	ENSP00000479931.1:n.457-140_457-139insCATG
NM_000136.2:c.457-140_457-139insCATG , LRG_497t1:c.457-140_457-139insCATG	NP_000127.2:n.457-140_457-139insCATG
NM_001243743.1:c.457-140_457-139insCATG	NP_001230672.1:n.457-140_457-139insCATG
NM_001243744.1:c.457-140_457-139insCATG	NP_001230673.1:n.457-140_457-139insCATG
XM_006717001.1:c.457-140_457-139insCATG	XP_006717064.1:n.457-140_457-139insCATG
XM_006717002.2:c.457-140_457-139insCATG	XP_006717065.1:n.457-140_457-139insCATG
XM_006717004.2:c.457-140_457-139insCATG	XP_006717067.1:n.457-140_457-139insCATG
XM_011518365.1:c.457-140_457-139insCATG	XP_011516667.1:n.457-140_457-139insCATG
XM_011518366.1:c.457-140_457-139insCATG	XP_011516668.1:n.457-140_457-139insCATG
XM_011518367.1:c.1-140_1-139insCATG	XP_011516669.1:n.1-140_1-139insCATG
XM_006717001.3:c.457-140_457-139insCATG	XP_006717064.1:n.457-140_457-139insCATG
XM_006717002.4:c.457-140_457-139insCATG	XP_006717065.1:n.457-140_457-139insCATG
XM_006717004.4:c.457-140_457-139insCATG	XP_006717067.1:n.457-140_457-139insCATG
XM_011518365.3:c.457-140_457-139insCATG	XP_011516667.1:n.457-140_457-139insCATG
XM_011518366.3:c.457-140_457-139insCATG	XP_011516668.1:n.457-140_457-139insCATG
XM_011518367.2:c.1-140_1-139insCATG	XP_011516669.1:n.1-140_1-139insCATG
XM_017014452.2:c.1-140_1-139insCATG	XP_016869941.1:n.1-140_1-139insCATG
XM_017014453.1:c.1-140_1-139insCATG	XP_016869942.1:n.1-140_1-139insCATG
XM_017014454.1:c.1-140_1-139insCATG	XP_016869943.1:n.1-140_1-139insCATG
XM_024447451.1:c.457-140_457-139insCATG	XP_024303219.1:n.457-140_457-139insCATG
NM_000136.3:c.457-140_457-139insCATG MANE Select	NP_000127.2:n.457-140_457-139insCATG
NM_001243743.2:c.457-140_457-139insCATG	NP_001230672.1:n.457-140_457-139insCATG
NM_001243744.2:c.457-140_457-139insCATG	NP_001230673.1:n.457-140_457-139insCATG