Canonical Allele Identifier: CA1160469874
Gene: FCN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.27373182dup , CM000663.2:g.27373182dup GRCh38
NC_000001.10:g.27699673dup , CM000663.1:g.27699673dup GRCh37
NC_000001.9:g.27572260dup NCBI36
NG_016279.1:g.6645dup , LRG_171:g.6645dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000699962.1:n.348dup
ENST00000699963.1:c.349dup ENSP00000514719.1:p.Leu117ProfsTer6
ENST00000270879.9:c.349dup MANE Select ENSP00000270879.4:p.Leu117ProfsTer6
ENST00000270879.8:c.349dup ENSP00000270879.4:p.Leu117ProfsTer6
ENST00000354982.2:c.316dup ENSP00000347077.2:p.Leu106ProfsTer6
ENST00000498393.1:n.499dup
NM_003665.2:c.349dup , LRG_171t1:c.349dup NP_003656.2:p.Leu117ProfsTer6
NM_173452.1:c.316dup NP_775628.1:p.Leu106ProfsTer6
XM_011542339.1:c.349dup XP_011540641.1:p.Leu117ProfsTer6
NM_003665.3:c.349dup NP_003656.2:p.Leu117ProfsTer6
NM_173452.2:c.316dup NP_775628.1:p.Leu106ProfsTer6
NM_003665.4:c.349dup MANE Select NP_003656.2:p.Leu117ProfsTer6
NM_173452.3:c.316dup NP_775628.1:p.Leu106ProfsTer6