Canonical Allele Identifier: CA1865515618

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95249382_95249386delinsGAACA , CM000671.2:g.95249382_95249386delinsGAACA	GRCh38
NC_000009.11:g.98011664_98011668delinsGAACA , CM000671.1:g.98011664_98011668delinsGAACA	GRCh37
NC_000009.10:g.97051485_97051489delinsGAACA	NCBI36
NG_011707.1:g.73324_73328delinsTGTTC , LRG_497:g.73324_73328delinsTGTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000696261.1:n.169-17_169-13delinsTGTTC
ENST00000696262.1:c.-78-17_-78-13delinsTGTTC	ENSP00000512510.1:n.-78-17_-78-13delinsTG...
ENST00000696263.1:n.178-17_178-13delinsTGTTC
ENST00000289081.8:c.-78-17_-78-13delinsTGTTC MANE Select	ENSP00000289081.3:n.-78-17_-78-13delinsTG...
ENST00000375305.6:c.-78-17_-78-13delinsTGTTC	ENSP00000364454.1:n.-78-17_-78-13delinsTG...
ENST00000490972.7:c.-78-17_-78-13delinsTGTTC	ENSP00000479931.1:n.-78-17_-78-13delinsTG...
ENST00000636777.1:n.20-56_20-52delinsTGTTC
ENST00000647778.1:c.-78-17_-78-13delinsTGTTC	ENSP00000498125.1:n.-78-17_-78-13delinsTG...
ENST00000647882.1:c.-78-17_-78-13delinsTGTTC	ENSP00000497025.1:n.-78-17_-78-13delinsTG...
ENST00000648415.1:n.1561-17_1561-13delinsTGTTC
ENST00000649519.1:c.-78-17_-78-13delinsTGTTC	ENSP00000497630.1:n.-78-17_-78-13delinsTG...
ENST00000649611.1:c.-78-17_-78-13delinsTGTTC	ENSP00000497986.1:n.-78-17_-78-13delinsTG...
ENST00000650176.1:n.103-17_103-13delinsTGTTC
ENST00000289081.7:c.-78-17_-78-13delinsTGTTC	ENSP00000289081.3:n.-78-17_-78-13delinsTG...
ENST00000375305.5:c.-78-17_-78-13delinsTGTTC	ENSP00000364454.1:n.-78-17_-78-13delinsTG...
ENST00000433829.1:c.-78-17_-78-13delinsTGTTC	ENSP00000406908.1:n.-78-17_-78-13delinsTG...
ENST00000474949.1:n.185-17_185-13delinsTGTTC
ENST00000490972.6:c.-78-17_-78-13delinsTGTTC	ENSP00000479931.1:n.-78-17_-78-13delinsTG...
NM_000136.2:c.-78-17_-78-13delinsTGTTC , LRG_497t1:c.-78-17_-78-13delinsTGTTC	NP_000127.2:n.-78-17_-78-13delinsTGTTC
NM_001243743.1:c.-78-17_-78-13delinsTGTTC	NP_001230672.1:n.-78-17_-78-13delinsTGTTC...
NM_001243744.1:c.-78-17_-78-13delinsTGTTC	NP_001230673.1:n.-78-17_-78-13delinsTGTTC...
XM_006717001.1:c.-78-17_-78-13delinsTGTTC	XP_006717064.1:n.-78-17_-78-13delinsTGTTC...
XM_006717002.2:c.-78-17_-78-13delinsTGTTC	XP_006717065.1:n.-78-17_-78-13delinsTGTTC...
XM_006717004.2:c.-78-17_-78-13delinsTGTTC	XP_006717067.1:n.-78-17_-78-13delinsTGTTC...
XM_011518365.1:c.-78-17_-78-13delinsTGTTC	XP_011516667.1:n.-78-17_-78-13delinsTGTTC...
XM_011518366.1:c.-78-17_-78-13delinsTGTTC	XP_011516668.1:n.-78-17_-78-13delinsTGTTC...
XM_011518367.1:c.-679-17_-679-13delinsTGTTC	XP_011516669.1:n.-679-17_-679-13delinsTGT...
XM_006717001.3:c.-78-17_-78-13delinsTGTTC	XP_006717064.1:n.-78-17_-78-13delinsTGTTC...
XM_006717002.4:c.-78-17_-78-13delinsTGTTC	XP_006717065.1:n.-78-17_-78-13delinsTGTTC...
XM_006717004.4:c.-78-17_-78-13delinsTGTTC	XP_006717067.1:n.-78-17_-78-13delinsTGTTC...
XM_011518365.3:c.-78-17_-78-13delinsTGTTC	XP_011516667.1:n.-78-17_-78-13delinsTGTTC...
XM_011518366.3:c.-78-17_-78-13delinsTGTTC	XP_011516668.1:n.-78-17_-78-13delinsTGTTC...
XM_011518367.2:c.-679-17_-679-13delinsTGTTC	XP_011516669.1:n.-679-17_-679-13delinsTGT...
XM_017014452.2:c.-679-17_-679-13delinsTGTTC	XP_016869941.1:n.-679-17_-679-13delinsTGT...
XM_017014453.1:c.-679-17_-679-13delinsTGTTC	XP_016869942.1:n.-679-17_-679-13delinsTGT...
XM_017014454.1:c.-679-17_-679-13delinsTGTTC	XP_016869943.1:n.-679-17_-679-13delinsTGT...
XM_024447451.1:c.-78-17_-78-13delinsTGTTC	XP_024303219.1:n.-78-17_-78-13delinsTGTTC...
NM_000136.3:c.-78-17_-78-13delinsTGTTC MANE Select	NP_000127.2:n.-78-17_-78-13delinsTGTTC
NM_001243743.2:c.-78-17_-78-13delinsTGTTC	NP_001230672.1:n.-78-17_-78-13delinsTGTTC...
NM_001243744.2:c.-78-17_-78-13delinsTGTTC	NP_001230673.1:n.-78-17_-78-13delinsTGTTC...