Canonical Allele Identifier: CA913189756

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95247433_95249292del , CM000671.2:g.95247433_95249292del	GRCh38
NC_000009.11:g.98009715_98011574del , CM000671.1:g.98009715_98011574del	GRCh37
NC_000009.10:g.97049536_97051395del	NCBI36
NG_011707.1:g.73419_75278del , LRG_497:g.73419_75278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.247_496del
ENST00000696262.1:c.1_250del
ENST00000289081.8:c.1_250del
ENST00000375305.6:c.1_250del
ENST00000490972.7:c.1_250del
ENST00000636777.1:n.59_308del
ENST00000647778.1:c.1_250del
ENST00000647882.1:c.1_250del
ENST00000648415.1:n.1639_1888del
ENST00000649519.1:c.1_250del
ENST00000650176.1:n.181_430del
ENST00000289081.7:c.1_250del
ENST00000375305.5:c.1_250del
ENST00000433829.1:c.1_250del
ENST00000474949.1:n.263_512del
ENST00000490972.6:c.1_250del
NM_000136.2:c.1_250del , LRG_497t1:c.1_250del
NM_001243743.1:c.1_250del
NM_001243744.1:c.1_250del
XM_006717001.1:c.1_250del
XM_006717002.2:c.1_250del
XM_006717004.2:c.1_250del
XM_011518365.1:c.1_250del
XM_011518366.1:c.1_250del
XM_011518367.1:c.-601_-352del
XM_006717001.3:c.1_250del
XM_006717002.4:c.1_250del
XM_006717004.4:c.1_250del
XM_011518365.3:c.1_250del
XM_011518366.3:c.1_250del
XM_011518367.2:c.-601_-352del
XM_017014452.2:c.-601_-352del
XM_017014453.1:c.-601_-352del
XM_017014454.1:c.-601_-352del
XM_024447451.1:c.1_250del
NM_000136.3:c.1_250del
NM_001243743.2:c.1_250del
NM_001243744.2:c.1_250del