Canonical Allele Identifier: CA374338587
Gene: FANCC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95171101T>G , CM000671.2:g.95171101T>G GRCh38
NC_000009.11:g.97933383T>G , CM000671.1:g.97933383T>G GRCh37
NC_000009.10:g.96973204T>G NCBI36
NG_011707.1:g.151609A>C , LRG_497:g.151609A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696261.1:n.890A>C
ENST00000289081.8:c.499A>C MANE Select ENSP00000289081.3:p.Asn167His
ENST00000375305.6:c.499A>C ENSP00000364454.1:p.Asn167His
ENST00000490972.7:c.499A>C ENSP00000479931.1:p.Asn167His
ENST00000636777.1:n.557A>C
ENST00000649334.1:c.644A>C ENSP00000497735.1:n.644A>C
ENST00000649701.1:n.214A>C
ENST00000289081.7:c.499A>C ENSP00000289081.3:p.Asn167His
ENST00000375305.5:c.499A>C ENSP00000364454.1:p.Asn167His
ENST00000490972.6:c.499A>C ENSP00000479931.1:p.Asn167His
NM_000136.2:c.499A>C , LRG_497t1:c.499A>C NP_000127.2:p.Asn167His
NM_001243743.1:c.499A>C NP_001230672.1:p.Asn167His
NM_001243744.1:c.499A>C NP_001230673.1:p.Asn167His
XM_006717001.1:c.499A>C XP_006717064.1:p.Asn167His
XM_006717002.2:c.499A>C XP_006717065.1:p.Asn167His
XM_006717004.2:c.499A>C XP_006717067.1:p.Asn167His
XM_011518365.1:c.499A>C XP_011516667.1:p.Asn167His
XM_011518366.1:c.499A>C XP_011516668.1:p.Asn167His
XM_011518367.1:c.43A>C XP_011516669.1:p.Asn15His
XM_006717001.3:c.499A>C XP_006717064.1:p.Asn167His
XM_006717002.4:c.499A>C XP_006717065.1:p.Asn167His
XM_006717004.4:c.499A>C XP_006717067.1:p.Asn167His
XM_011518365.3:c.499A>C XP_011516667.1:p.Asn167His
XM_011518366.3:c.499A>C XP_011516668.1:p.Asn167His
XM_011518367.2:c.43A>C XP_011516669.1:p.Asn15His
XM_017014452.2:c.43A>C XP_016869941.1:p.Asn15His
XM_017014453.1:c.43A>C XP_016869942.1:p.Asn15His
XM_017014454.1:c.43A>C XP_016869943.1:p.Asn15His
XM_024447451.1:c.499A>C XP_024303219.1:p.Asn167His
NM_000136.3:c.499A>C MANE Select NP_000127.2:p.Asn167His
NM_001243743.2:c.499A>C NP_001230672.1:p.Asn167His
NM_001243744.2:c.499A>C NP_001230673.1:p.Asn167His