Canonical Allele Identifier: CA2655998265
Gene: RASL10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313226del , CM000684.2:g.29313226del GRCh38
NC_000022.10:g.29709215del , CM000684.1:g.29709215del GRCh37
NC_000022.9:g.28039215del NCBI36
NG_032959.1:g.11220del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*77del MANE Select ENSP00000216101.6:n.*77del
ENST00000216101.6:c.*77del ENSP00000216101.6:n.*77del
ENST00000401450.3:c.*635del ENSP00000386095.3:n.*635del
NM_006477.4:c.*77del NP_006468.1:n.*77del
XM_011529821.1:c.*77del XP_011528123.1:n.*77del
XM_011529822.1:c.*77del XP_011528124.1:n.*77del
XM_011529823.1:c.*77del XP_011528125.1:n.*77del
NM_006477.5:c.*77del MANE Select NP_006468.1:n.*77del