Canonical Allele Identifier: CA2655998331
Gene: RASL10A HGNC NCBI

Linked Data

gnomAD v4: 22-29313256-TCCCAGTCACAAGGTGGGGCCCATGGATGGCACTGTCCGATCGGGTCACATGAGGCTGCAGCGCGCGGGATGCAGCGCCCCCTGCAGGCGCAGGGCCGGGTGTGCAGGGCGCGCGCGCA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313259_29313376del , CM000684.2:g.29313259_29313376del GRCh38
NC_000022.10:g.29709248_29709365del , CM000684.1:g.29709248_29709365del GRCh37
NC_000022.9:g.28039248_28039365del NCBI36
NG_032959.1:g.11253_11370del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.539_*44del MANE Select ENSP00000216101.6:n.[c.539_*44del;Val180AspfsTer24]
ENST00000216101.6:c.539_*44del ENSP00000216101.6:n.[c.539_*44del;Val180AspfsTer24]
ENST00000401450.3:c.*485_*602del ENSP00000386095.3:n.*485_*602del
NM_006477.4:c.539_*44del NP_006468.1:n.[c.539_*44del;Val180AspfsTer24]
XM_011529821.1:c.599_*44del XP_011528123.1:n.[c.599_*44del;Val200AspfsTer24]
XM_011529822.1:c.599_*44del XP_011528124.1:n.[c.599_*44del;Val200AspfsTer24]
XM_011529823.1:c.395_*44del XP_011528125.1:n.[c.395_*44del;Val132AspfsTer24]
NM_006477.5:c.539_*44del MANE Select NP_006468.1:n.[c.539_*44del;Val180AspfsTer24]
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