Canonical Allele Identifier: CA1592781297
Gene: SAP30L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154457496T= , CM000667.2:g.154457496T= GRCh38
NC_000005.9:g.153837056T= , CM000667.1:g.153837056T= GRCh37
NC_000005.8:g.153817249T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297109.11:c.*1468T= MANE Select ENSP00000297109.5:n.*1468T=
ENST00000297109.10:c.*1468T= ENSP00000297109.5:n.*1468T=
NM_001131062.1:c.*1468T= NP_001124534.1:n.*1468T=
NM_001131063.1:c.*1468T= NP_001124535.1:n.*1468T=
NM_024632.5:c.*1468T= NP_078908.1:n.*1468T=
NR_024084.1:n.2712T=
NM_024632.6:c.*1468T= MANE Select NP_078908.1:n.*1468T=
NM_001131062.2:c.*1468T= NP_001124534.1:n.*1468T=
NM_001131063.2:c.*1468T= NP_001124535.1:n.*1468T=
NR_024084.2:n.2672T=
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