Canonical Allele Identifier: CA1592781298
Gene: SAP30L HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154457498T= , CM000667.2:g.154457498T= GRCh38
NC_000005.9:g.153837058T= , CM000667.1:g.153837058T= GRCh37
NC_000005.8:g.153817251T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297109.11:c.*1470T= MANE Select ENSP00000297109.5:n.*1470T=
ENST00000297109.10:c.*1470T= ENSP00000297109.5:n.*1470T=
NM_001131062.1:c.*1470T= NP_001124534.1:n.*1470T=
NM_001131063.1:c.*1470T= NP_001124535.1:n.*1470T=
NM_024632.5:c.*1470T= NP_078908.1:n.*1470T=
NR_024084.1:n.2714T=
NM_024632.6:c.*1470T= MANE Select NP_078908.1:n.*1470T=
NM_001131062.2:c.*1470T= NP_001124534.1:n.*1470T=
NM_001131063.2:c.*1470T= NP_001124535.1:n.*1470T=
NR_024084.2:n.2674T=
Search 100 bp 5'
Search 100 bp 3'