Canonical Allele Identifier: CA1865483121

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171132_95171133delinsTG , CM000671.2:g.95171132_95171133delinsTG	GRCh38
NC_000009.11:g.97933414_97933415delinsTG , CM000671.1:g.97933414_97933415delinsTG	GRCh37
NC_000009.10:g.96973235_96973236delinsTG	NCBI36
NG_011707.1:g.151577_151578delinsCA , LRG_497:g.151577_151578delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.858_859delinsCA
ENST00000289081.8:c.467_468delinsCA MANE Select	ENSP00000289081.3:p.Ser156=
ENST00000375305.6:c.467_468delinsCA	ENSP00000364454.1:p.Ser156=
ENST00000490972.7:c.467_468delinsCA	ENSP00000479931.1:p.Ser156=
ENST00000636777.1:n.525_526delinsCA
ENST00000649334.1:c.612_613delinsCA	ENSP00000497735.1:n.612_613delinsCA
ENST00000649701.1:n.182_183delinsCA
ENST00000289081.7:c.467_468delinsCA	ENSP00000289081.3:p.Ser156=
ENST00000375305.5:c.467_468delinsCA	ENSP00000364454.1:p.Ser156=
ENST00000474949.1:n.824_825delinsCA
ENST00000490972.6:c.467_468delinsCA	ENSP00000479931.1:p.Ser156=
NM_000136.2:c.467_468delinsCA , LRG_497t1:c.467_468delinsCA	NP_000127.2:p.Ser156=
NM_001243743.1:c.467_468delinsCA	NP_001230672.1:p.Ser156=
NM_001243744.1:c.467_468delinsCA	NP_001230673.1:p.Ser156=
XM_006717001.1:c.467_468delinsCA	XP_006717064.1:p.Ser156=
XM_006717002.2:c.467_468delinsCA	XP_006717065.1:p.Ser156=
XM_006717004.2:c.467_468delinsCA	XP_006717067.1:p.Ser156=
XM_011518365.1:c.467_468delinsCA	XP_011516667.1:p.Ser156=
XM_011518366.1:c.467_468delinsCA	XP_011516668.1:p.Ser156=
XM_011518367.1:c.11_12delinsCA	XP_011516669.1:p.Ser4=
XM_006717001.3:c.467_468delinsCA	XP_006717064.1:p.Ser156=
XM_006717002.4:c.467_468delinsCA	XP_006717065.1:p.Ser156=
XM_006717004.4:c.467_468delinsCA	XP_006717067.1:p.Ser156=
XM_011518365.3:c.467_468delinsCA	XP_011516667.1:p.Ser156=
XM_011518366.3:c.467_468delinsCA	XP_011516668.1:p.Ser156=
XM_011518367.2:c.11_12delinsCA	XP_011516669.1:p.Ser4=
XM_017014452.2:c.11_12delinsCA	XP_016869941.1:p.Ser4=
XM_017014453.1:c.11_12delinsCA	XP_016869942.1:p.Ser4=
XM_017014454.1:c.11_12delinsCA	XP_016869943.1:p.Ser4=
XM_024447451.1:c.467_468delinsCA	XP_024303219.1:p.Ser156=
NM_000136.3:c.467_468delinsCA MANE Select	NP_000127.2:p.Ser156=
NM_001243743.2:c.467_468delinsCA	NP_001230672.1:p.Ser156=
NM_001243744.2:c.467_468delinsCA	NP_001230673.1:p.Ser156=