Canonical Allele Identifier: CA2400518646
Gene: RASL10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29312936_29312939delinsAATT , CM000684.2:g.29312936_29312939delinsAATT GRCh38
NC_000022.10:g.29708925_29708928delinsAATT , CM000684.1:g.29708925_29708928delinsAATT GRCh37
NC_000022.9:g.28038925_28038928delinsAATT NCBI36
NG_032959.1:g.10930_10933delinsAATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*362_*365delinsAATT MANE Select ENSP00000216101.6:n.*362_*365delinsAATT
ENST00000216101.6:c.*362_*365delinsAATT ENSP00000216101.6:n.*362_*365delinsAATT
ENST00000401450.3:c.*920_*923delinsAATT ENSP00000386095.3:n.*920_*923delinsAATT
NM_006477.4:c.*362_*365delinsAATT NP_006468.1:n.*362_*365delinsAATT
XM_011529821.1:c.*362_*365delinsAATT XP_011528123.1:n.*362_*365delinsAATT
XM_011529822.1:c.*362_*365delinsAATT XP_011528124.1:n.*362_*365delinsAATT
XM_011529823.1:c.*362_*365delinsAATT XP_011528125.1:n.*362_*365delinsAATT
NM_006477.5:c.*362_*365delinsAATT MANE Select NP_006468.1:n.*362_*365delinsAATT