Canonical Allele Identifier: CA1592781295
Gene: SAP30L HGNC NCBI

Linked Data

dbSNP Id: rs1757287919

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154457490A>T , CM000667.2:g.154457490A>T GRCh38
NC_000005.9:g.153837050A>T , CM000667.1:g.153837050A>T GRCh37
NC_000005.8:g.153817243A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297109.11:c.*1462A>T MANE Select ENSP00000297109.5:n.*1462A>T
ENST00000297109.10:c.*1462A>T ENSP00000297109.5:n.*1462A>T
NM_001131062.1:c.*1462A>T NP_001124534.1:n.*1462A>T
NM_001131063.1:c.*1462A>T NP_001124535.1:n.*1462A>T
NM_024632.5:c.*1462A>T NP_078908.1:n.*1462A>T
NR_024084.1:n.2706A>T
NM_024632.6:c.*1462A>T MANE Select NP_078908.1:n.*1462A>T
NM_001131062.2:c.*1462A>T NP_001124534.1:n.*1462A>T
NM_001131063.2:c.*1462A>T NP_001124535.1:n.*1462A>T
NR_024084.2:n.2666A>T