Canonical Allele Identifier: CA2508754483
Gene: RASL10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313222_29313224del , CM000684.2:g.29313222_29313224del GRCh38
NC_000022.10:g.29709211_29709213del , CM000684.1:g.29709211_29709213del GRCh37
NC_000022.9:g.28039211_28039213del NCBI36
NG_032959.1:g.11216_11218del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*78_*80del MANE Select ENSP00000216101.6:n.*78_*80del
ENST00000216101.6:c.*78_*80del ENSP00000216101.6:n.*78_*80del
ENST00000401450.3:c.*636_*638del ENSP00000386095.3:n.*636_*638del
NM_006477.4:c.*78_*80del NP_006468.1:n.*78_*80del
XM_011529821.1:c.*78_*80del XP_011528123.1:n.*78_*80del
XM_011529822.1:c.*78_*80del XP_011528124.1:n.*78_*80del
XM_011529823.1:c.*78_*80del XP_011528125.1:n.*78_*80del
NM_006477.5:c.*78_*80del MANE Select NP_006468.1:n.*78_*80del