Canonical Allele Identifier: CA374106014

Linked Data

ClinVar Variation Id: 1772300
ClinVar RCV Id: RCV002391862

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95107176T>G , CM000671.2:g.95107176T>G GRCh38
NC_000009.11:g.97869458T>G , CM000671.1:g.97869458T>G GRCh37
NC_000009.10:g.96909279T>G NCBI36
NG_011707.1:g.215534A>C , LRG_497:g.215534A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000710812.1:n.410+26396T>G (AOPEP)
ENST00000696260.1:n.2238A>C (FANCC)
ENST00000289081.8:c.1423A>C (FANCC) MANE Select ENSP00000289081.3:p.Thr475Pro
ENST00000375305.6:c.1423A>C (FANCC) ENSP00000364454.1:p.Thr475Pro
ENST00000649334.1:c.1568A>C (FANCC) ENSP00000497735.1:n.1568A>C
ENST00000289081.7:c.1423A>C (FANCC) ENSP00000289081.3:p.Thr475Pro
ENST00000375305.5:c.1423A>C (FANCC) ENSP00000364454.1:p.Thr475Pro
ENST00000464627.5:n.750A>C (FANCC)
NM_000136.2:c.1423A>C , LRG_497t1:c.1423A>C (FANCC) NP_000127.2:p.Thr475Pro
NM_001243743.1:c.1423A>C (FANCC) NP_001230672.1:p.Thr475Pro
XM_005251802.2:c.742A>C (FANCC) XP_005251859.1:p.Thr248Pro
XM_006717001.1:c.1258A>C (FANCC) XP_006717064.1:p.Thr420Pro
XM_011518365.1:c.1423A>C (FANCC) XP_011516667.1:p.Thr475Pro
XM_011518367.1:c.967A>C (FANCC) XP_011516669.1:p.Thr323Pro
XM_011519121.1:c.2319+26396T>G (AOPEP) XP_011517423.1:n.2319+26396T>G
XM_005251802.3:c.742A>C (FANCC) XP_005251859.1:p.Thr248Pro
XM_006717001.3:c.1258A>C (FANCC) XP_006717064.1:p.Thr420Pro
XM_011518365.3:c.1423A>C (FANCC) XP_011516667.1:p.Thr475Pro
XM_011518367.2:c.967A>C (FANCC) XP_011516669.1:p.Thr323Pro
XM_011519121.3:c.2319+26396T>G (AOPEP) XP_011517423.1:n.2319+26396T>G
XM_017014452.2:c.967A>C (FANCC) XP_016869941.1:p.Thr323Pro
XM_017014453.1:c.967A>C (FANCC) XP_016869942.1:p.Thr323Pro
XM_017014454.1:c.802A>C (FANCC) XP_016869943.1:p.Thr268Pro
XM_024447451.1:c.1423A>C (FANCC) XP_024303219.1:p.Thr475Pro
XR_001746847.1:n.594T>G
NM_000136.3:c.1423A>C (FANCC) MANE Select NP_000127.2:p.Thr475Pro
NM_001243743.2:c.1423A>C (FANCC) NP_001230672.1:p.Thr475Pro