Canonical Allele Identifier: CA2321352938
Gene: CD320 HGNC NCBI
ELAVL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8305041_8305043dup , CM000681.2:g.8305041_8305043dup GRCh38
NC_000019.9:g.8369925_8369927dup , CM000681.1:g.8369925_8369927dup GRCh37
NC_000019.8:g.8275925_8275927dup NCBI36
NG_028124.1:g.8320_8322dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301458.10:c.262_264dup (CD320) MANE Select ENSP00000301458.4:p.Glu88_Cys89insGlu
ENST00000301458.9:c.262_264dup (CD320) ENSP00000301458.4:p.Glu88_Cys89insGlu
ENST00000351593.9:c.-87-43033_-87-43031dup (ELAVL1) ENSP00000264073.6:n.-87-43033_-87-43031dup
ENST00000537716.6:c.143-949_143-947dup (CD320) ENSP00000437697.1:n.143-949_143-947dup
ENST00000596002.5:c.*665_*667dup (CD320) ENSP00000471773.1:n.*665_*667dup
ENST00000598299.1:n.307_309dup (CD320)
ENST00000599573.1:c.243_245dup (CD320)
NM_001165895.1:c.143-949_143-947dup (CD320) NP_001159367.1:n.143-949_143-947dup
NM_016579.3:c.262_264dup (CD320) NP_057663.1:p.Glu88_Cys89insGlu
NM_016579.4:c.262_264dup (CD320) MANE Select NP_057663.1:p.Glu88_Cys89insGlu
NM_001165895.2:c.143-949_143-947dup (CD320) NP_001159367.1:n.143-949_143-947dup
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