Canonical Allele Identifier: CA374105700

Linked Data

dbSNP Id: rs2134455010

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95107121T>A , CM000671.2:g.95107121T>A GRCh38
NC_000009.11:g.97869403T>A , CM000671.1:g.97869403T>A GRCh37
NC_000009.10:g.96909224T>A NCBI36
NG_011707.1:g.215589A>T , LRG_497:g.215589A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710812.1:n.410+26341T>A (AOPEP)
ENST00000696260.1:n.2293A>T (FANCC)
ENST00000289081.8:c.1478A>T (FANCC) MANE Select ENSP00000289081.3:p.Asn493Ile
ENST00000375305.6:c.1478A>T (FANCC) ENSP00000364454.1:p.Asn493Ile
ENST00000649334.1:c.1623A>T (FANCC) ENSP00000497735.1:n.1623A>T
ENST00000289081.7:c.1478A>T (FANCC) ENSP00000289081.3:p.Asn493Ile
ENST00000375305.5:c.1478A>T (FANCC) ENSP00000364454.1:p.Asn493Ile
ENST00000464627.5:n.805A>T (FANCC)
NM_000136.2:c.1478A>T , LRG_497t1:c.1478A>T (FANCC) NP_000127.2:p.Asn493Ile
NM_001243743.1:c.1478A>T (FANCC) NP_001230672.1:p.Asn493Ile
XM_005251802.2:c.797A>T (FANCC) XP_005251859.1:p.Asn266Ile
XM_006717001.1:c.1313A>T (FANCC) XP_006717064.1:p.Asn438Ile
XM_011518365.1:c.1478A>T (FANCC) XP_011516667.1:p.Asn493Ile
XM_011518367.1:c.1022A>T (FANCC) XP_011516669.1:p.Asn341Ile
XM_011519121.1:c.2319+26341T>A (AOPEP) XP_011517423.1:n.2319+26341T>A
XM_005251802.3:c.797A>T (FANCC) XP_005251859.1:p.Asn266Ile
XM_006717001.3:c.1313A>T (FANCC) XP_006717064.1:p.Asn438Ile
XM_011518365.3:c.1478A>T (FANCC) XP_011516667.1:p.Asn493Ile
XM_011518367.2:c.1022A>T (FANCC) XP_011516669.1:p.Asn341Ile
XM_011519121.3:c.2319+26341T>A (AOPEP) XP_011517423.1:n.2319+26341T>A
XM_017014452.2:c.1022A>T (FANCC) XP_016869941.1:p.Asn341Ile
XM_017014453.1:c.1022A>T (FANCC) XP_016869942.1:p.Asn341Ile
XM_017014454.1:c.857A>T (FANCC) XP_016869943.1:p.Asn286Ile
XM_024447451.1:c.1478A>T (FANCC) XP_024303219.1:p.Asn493Ile
XR_001746847.1:n.539T>A
NM_000136.3:c.1478A>T (FANCC) MANE Select NP_000127.2:p.Asn493Ile
NM_001243743.2:c.1478A>T (FANCC) NP_001230672.1:p.Asn493Ile