Canonical Allele Identifier: CA752236983
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs1352055612
gnomAD v3: 22-29313252-AT-A
gnomAD v4: 22-29313252-AT-A
MyVariant Identifiers: chr22:g.29709242del (hg19) chr22:g.29313253del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313254del , CM000684.2:g.29313254del GRCh38
NC_000022.10:g.29709243del , CM000684.1:g.29709243del GRCh37
NC_000022.9:g.28039243del NCBI36
NG_032959.1:g.11248del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*48del MANE Select ENSP00000216101.6:n.*48del
ENST00000216101.6:c.*48del ENSP00000216101.6:n.*48del
ENST00000401450.3:c.*606del ENSP00000386095.3:n.*606del
NM_006477.4:c.*48del NP_006468.1:n.*48del
XM_011529821.1:c.*48del XP_011528123.1:n.*48del
XM_011529822.1:c.*48del XP_011528124.1:n.*48del
XM_011529823.1:c.*48del XP_011528125.1:n.*48del
NM_006477.5:c.*48del MANE Select NP_006468.1:n.*48del
Search 100 bp 5'
Search 100 bp 3'