Canonical Allele Identifier: CA1865483753

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95172132_95172137delinsTATGAG , CM000671.2:g.95172132_95172137delinsTATGAG	GRCh38
NC_000009.11:g.97934414_97934419delinsTATGAG , CM000671.1:g.97934414_97934419delinsTATGAG	GRCh37
NC_000009.10:g.96974235_96974240delinsTATGAG	NCBI36
NG_011707.1:g.150573_150578delinsCTCATA , LRG_497:g.150573_150578delinsCTCATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.747_752delinsCTCATA
ENST00000289081.8:c.356_361delinsCTCATA MANE Select	ENSP00000289081.3:p.Ser119=
ENST00000375305.6:c.356_361delinsCTCATA	ENSP00000364454.1:p.Ser119=
ENST00000490972.7:c.356_361delinsCTCATA	ENSP00000479931.1:p.Ser119=
ENST00000636777.1:n.414_419delinsCTCATA
ENST00000647778.1:c.356_361delinsCTCATA	ENSP00000498125.1:p.Ser119=
ENST00000647882.1:c.356_361delinsCTCATA	ENSP00000497025.1:p.Ser119=
ENST00000649334.1:c.501_506delinsCTCATA	ENSP00000497735.1:n.501_506delinsCTCATA
ENST00000649701.1:n.71_76delinsCTCATA
ENST00000289081.7:c.356_361delinsCTCATA	ENSP00000289081.3:p.Ser119=
ENST00000375305.5:c.356_361delinsCTCATA	ENSP00000364454.1:p.Ser119=
ENST00000433829.1:c.356_361delinsCTCATA	ENSP00000406908.1:p.Ser119=
ENST00000474949.1:n.713_718delinsCTCATA
ENST00000490972.6:c.356_361delinsCTCATA	ENSP00000479931.1:p.Ser119=
NM_000136.2:c.356_361delinsCTCATA , LRG_497t1:c.356_361delinsCTCATA	NP_000127.2:p.Ser119=
NM_001243743.1:c.356_361delinsCTCATA	NP_001230672.1:p.Ser119=
NM_001243744.1:c.356_361delinsCTCATA	NP_001230673.1:p.Ser119=
XM_006717001.1:c.356_361delinsCTCATA	XP_006717064.1:p.Ser119=
XM_006717002.2:c.356_361delinsCTCATA	XP_006717065.1:p.Ser119=
XM_006717004.2:c.356_361delinsCTCATA	XP_006717067.1:p.Ser119=
XM_011518365.1:c.356_361delinsCTCATA	XP_011516667.1:p.Ser119=
XM_011518366.1:c.356_361delinsCTCATA	XP_011516668.1:p.Ser119=
XM_011518367.1:c.-101_-96delinsCTCATA	XP_011516669.1:n.-101_-96delinsCTCATA
XM_006717001.3:c.356_361delinsCTCATA	XP_006717064.1:p.Ser119=
XM_006717002.4:c.356_361delinsCTCATA	XP_006717065.1:p.Ser119=
XM_006717004.4:c.356_361delinsCTCATA	XP_006717067.1:p.Ser119=
XM_011518365.3:c.356_361delinsCTCATA	XP_011516667.1:p.Ser119=
XM_011518366.3:c.356_361delinsCTCATA	XP_011516668.1:p.Ser119=
XM_011518367.2:c.-101_-96delinsCTCATA	XP_011516669.1:n.-101_-96delinsCTCATA
XM_017014452.2:c.-101_-96delinsCTCATA	XP_016869941.1:n.-101_-96delinsCTCATA
XM_017014453.1:c.-101_-96delinsCTCATA	XP_016869942.1:n.-101_-96delinsCTCATA
XM_017014454.1:c.-101_-96delinsCTCATA	XP_016869943.1:n.-101_-96delinsCTCATA
XM_024447451.1:c.356_361delinsCTCATA	XP_024303219.1:p.Ser119=
NM_000136.3:c.356_361delinsCTCATA MANE Select	NP_000127.2:p.Ser119=
NM_001243743.2:c.356_361delinsCTCATA	NP_001230672.1:p.Ser119=
NM_001243744.2:c.356_361delinsCTCATA	NP_001230673.1:p.Ser119=