Canonical Allele Identifier: CA374338555

Gene: FANCC

Linked Data

• dbSNP Id: rs2135578461
• MyVariant Identifiers: chr9:g.97933370G>A (hg19) ; chr9:g.95171088G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171088G>A , CM000671.2:g.95171088G>A	GRCh38
NC_000009.11:g.97933370G>A , CM000671.1:g.97933370G>A	GRCh37
NC_000009.10:g.96973191G>A	NCBI36
NG_011707.1:g.151622C>T , LRG_497:g.151622C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.903C>T
ENST00000289081.8:c.512C>T MANE Select	ENSP00000289081.3:p.Thr171Ile
ENST00000375305.6:c.512C>T	ENSP00000364454.1:p.Thr171Ile
ENST00000490972.7:c.512C>T	ENSP00000479931.1:p.Thr171Ile
ENST00000636777.1:n.570C>T
ENST00000649334.1:c.657C>T	ENSP00000497735.1:n.657C>T
ENST00000649701.1:n.227C>T
ENST00000289081.7:c.512C>T	ENSP00000289081.3:p.Thr171Ile
ENST00000375305.5:c.512C>T	ENSP00000364454.1:p.Thr171Ile
ENST00000490972.6:c.512C>T	ENSP00000479931.1:p.Thr171Ile
NM_000136.2:c.512C>T , LRG_497t1:c.512C>T	NP_000127.2:p.Thr171Ile
NM_001243743.1:c.512C>T	NP_001230672.1:p.Thr171Ile
NM_001243744.1:c.512C>T	NP_001230673.1:p.Thr171Ile
XM_006717001.1:c.512C>T	XP_006717064.1:p.Thr171Ile
XM_006717002.2:c.512C>T	XP_006717065.1:p.Thr171Ile
XM_006717004.2:c.512C>T	XP_006717067.1:p.Thr171Ile
XM_011518365.1:c.512C>T	XP_011516667.1:p.Thr171Ile
XM_011518366.1:c.512C>T	XP_011516668.1:p.Thr171Ile
XM_011518367.1:c.56C>T	XP_011516669.1:p.Thr19Ile
XM_006717001.3:c.512C>T	XP_006717064.1:p.Thr171Ile
XM_006717002.4:c.512C>T	XP_006717065.1:p.Thr171Ile
XM_006717004.4:c.512C>T	XP_006717067.1:p.Thr171Ile
XM_011518365.3:c.512C>T	XP_011516667.1:p.Thr171Ile
XM_011518366.3:c.512C>T	XP_011516668.1:p.Thr171Ile
XM_011518367.2:c.56C>T	XP_011516669.1:p.Thr19Ile
XM_017014452.2:c.56C>T	XP_016869941.1:p.Thr19Ile
XM_017014453.1:c.56C>T	XP_016869942.1:p.Thr19Ile
XM_017014454.1:c.56C>T	XP_016869943.1:p.Thr19Ile
XM_024447451.1:c.512C>T	XP_024303219.1:p.Thr171Ile
NM_000136.3:c.512C>T MANE Select	NP_000127.2:p.Thr171Ile
NM_001243743.2:c.512C>T	NP_001230672.1:p.Thr171Ile
NM_001243744.2:c.512C>T	NP_001230673.1:p.Thr171Ile