Canonical Allele Identifier: CA2690792493

Gene: FANCC

Linked Data

• gnomAD v4: 9-95240617-AAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95240621_95240623del , CM000671.2:g.95240621_95240623del	GRCh38
NC_000009.11:g.98002903_98002905del , CM000671.1:g.98002903_98002905del	GRCh37
NC_000009.10:g.97042724_97042726del	NCBI36
NG_011707.1:g.82090_82092del , LRG_497:g.82090_82092del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.591+29_591+31del
ENST00000696262.1:c.*17_*19del	ENSP00000512510.1:n.*17_*19del
ENST00000289081.8:c.345+29_345+31del MANE Select	ENSP00000289081.3:n.345+29_345+31del
ENST00000375305.6:c.345+29_345+31del	ENSP00000364454.1:n.345+29_345+31del
ENST00000490972.7:c.345+29_345+31del	ENSP00000479931.1:n.345+29_345+31del
ENST00000636777.1:n.403+29_403+31del
ENST00000647778.1:c.345+29_345+31del	ENSP00000498125.1:n.345+29_345+31del
ENST00000647882.1:c.345+29_345+31del	ENSP00000497025.1:n.345+29_345+31del
ENST00000648415.1:n.1983+29_1983+31del
ENST00000649334.1:c.345+29_345+31del	ENSP00000497735.1:n.345+29_345+31del
ENST00000649519.1:c.345+29_345+31del	ENSP00000497630.1:n.345+29_345+31del
ENST00000649701.1:n.60+29_60+31del
ENST00000649872.1:c.345+29_345+31del	ENSP00000497195.1:n.345+29_345+31del
ENST00000650176.1:n.525+29_525+31del
ENST00000289081.7:c.345+29_345+31del	ENSP00000289081.3:n.345+29_345+31del
ENST00000375305.5:c.345+29_345+31del	ENSP00000364454.1:n.345+29_345+31del
ENST00000433829.1:c.345+29_345+31del	ENSP00000406908.1:n.345+29_345+31del
ENST00000474949.1:n.607+29_607+31del
ENST00000490972.6:c.345+29_345+31del	ENSP00000479931.1:n.345+29_345+31del
NM_000136.2:c.345+29_345+31del , LRG_497t1:c.345+29_345+31del	NP_000127.2:n.345+29_345+31del
NM_001243743.1:c.345+29_345+31del	NP_001230672.1:n.345+29_345+31del
NM_001243744.1:c.345+29_345+31del	NP_001230673.1:n.345+29_345+31del
XM_006717001.1:c.345+29_345+31del	XP_006717064.1:n.345+29_345+31del
XM_006717002.2:c.345+29_345+31del	XP_006717065.1:n.345+29_345+31del
XM_006717004.2:c.345+29_345+31del	XP_006717067.1:n.345+29_345+31del
XM_011518365.1:c.345+29_345+31del	XP_011516667.1:n.345+29_345+31del
XM_011518366.1:c.345+29_345+31del	XP_011516668.1:n.345+29_345+31del
XM_011518367.1:c.-257+29_-257+31del	XP_011516669.1:n.-257+29_-257+31del
XM_006717001.3:c.345+29_345+31del	XP_006717064.1:n.345+29_345+31del
XM_006717002.4:c.345+29_345+31del	XP_006717065.1:n.345+29_345+31del
XM_006717004.4:c.345+29_345+31del	XP_006717067.1:n.345+29_345+31del
XM_011518365.3:c.345+29_345+31del	XP_011516667.1:n.345+29_345+31del
XM_011518366.3:c.345+29_345+31del	XP_011516668.1:n.345+29_345+31del
XM_011518367.2:c.-257+29_-257+31del	XP_011516669.1:n.-257+29_-257+31del
XM_017014452.2:c.-257+29_-257+31del	XP_016869941.1:n.-257+29_-257+31del
XM_017014453.1:c.-257+29_-257+31del	XP_016869942.1:n.-257+29_-257+31del
XM_017014454.1:c.-257+29_-257+31del	XP_016869943.1:n.-257+29_-257+31del
XM_024447451.1:c.345+29_345+31del	XP_024303219.1:n.345+29_345+31del
NM_000136.3:c.345+29_345+31del MANE Select	NP_000127.2:n.345+29_345+31del
NM_001243743.2:c.345+29_345+31del	NP_001230672.1:n.345+29_345+31del
NM_001243744.2:c.345+29_345+31del	NP_001230673.1:n.345+29_345+31del