Canonical Allele Identifier: CA2690785722

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95101835dup , CM000671.2:g.95101835dup GRCh38
NC_000009.11:g.97864117dup , CM000671.1:g.97864117dup GRCh37
NC_000009.10:g.96903938dup NCBI36
NG_011707.1:g.220875dup , LRG_497:g.220875dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000710812.1:n.410+21055dup (AOPEP)
ENST00000696260.1:n.2364dup (FANCC)
ENST00000289081.8:c.1549dup (FANCC) MANE Select ENSP00000289081.3:p.Glu517GlyfsTer11
ENST00000375305.6:c.1549dup (FANCC) ENSP00000364454.1:p.Glu517GlyfsTer11
ENST00000649334.1:c.1694dup (FANCC) ENSP00000497735.1:n.1694dup
ENST00000289081.7:c.1549dup (FANCC) ENSP00000289081.3:p.Glu517GlyfsTer11
ENST00000375305.5:c.1549dup (FANCC) ENSP00000364454.1:p.Glu517GlyfsTer11
NM_000136.2:c.1549dup , LRG_497t1:c.1549dup (FANCC) NP_000127.2:p.Glu517GlyfsTer11
NM_001243743.1:c.1549dup (FANCC) NP_001230672.1:p.Glu517GlyfsTer11
XM_005251802.2:c.868dup (FANCC) XP_005251859.1:p.Glu290GlyfsTer11
XM_006717001.1:c.1384dup (FANCC) XP_006717064.1:p.Glu462GlyfsTer11
XM_011518365.1:c.1549dup (FANCC) XP_011516667.1:p.Glu517GlyfsTer11
XM_011518367.1:c.1093dup (FANCC) XP_011516669.1:p.Glu365GlyfsTer11
XM_011519121.1:c.2319+21055dup (AOPEP) XP_011517423.1:n.2319+21055dup
XM_005251802.3:c.868dup (FANCC) XP_005251859.1:p.Glu290GlyfsTer11
XM_006717001.3:c.1384dup (FANCC) XP_006717064.1:p.Glu462GlyfsTer11
XM_011518365.3:c.1549dup (FANCC) XP_011516667.1:p.Glu517GlyfsTer11
XM_011518367.2:c.1093dup (FANCC) XP_011516669.1:p.Glu365GlyfsTer11
XM_011519121.3:c.2319+21055dup (AOPEP) XP_011517423.1:n.2319+21055dup
XM_017014452.2:c.1093dup (FANCC) XP_016869941.1:p.Glu365GlyfsTer11
XM_017014453.1:c.1093dup (FANCC) XP_016869942.1:p.Glu365GlyfsTer11
XM_017014454.1:c.928dup (FANCC) XP_016869943.1:p.Glu310GlyfsTer11
XM_024447451.1:c.1549dup (FANCC) XP_024303219.1:p.Glu517GlyfsTer11
NM_000136.3:c.1549dup (FANCC) MANE Select NP_000127.2:p.Glu517GlyfsTer11
NM_001243743.2:c.1549dup (FANCC) NP_001230672.1:p.Glu517GlyfsTer11