Canonical Allele Identifier: CA2400518651
Gene: RASL10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29312942T= , CM000684.2:g.29312942T= GRCh38
NC_000022.10:g.29708931T= , CM000684.1:g.29708931T= GRCh37
NC_000022.9:g.28038931T= NCBI36
NG_032959.1:g.10936T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*359A= MANE Select ENSP00000216101.6:n.*359A=
ENST00000216101.6:c.*359A= ENSP00000216101.6:n.*359A=
ENST00000401450.3:c.*917A= ENSP00000386095.3:n.*917A=
NM_006477.4:c.*359A= NP_006468.1:n.*359A=
XM_011529821.1:c.*359A= XP_011528123.1:n.*359A=
XM_011529822.1:c.*359A= XP_011528124.1:n.*359A=
XM_011529823.1:c.*359A= XP_011528125.1:n.*359A=
NM_006477.5:c.*359A= MANE Select NP_006468.1:n.*359A=