Canonical Allele Identifier: CA2400518645
Gene: RASL10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29312935A= , CM000684.2:g.29312935A= GRCh38
NC_000022.10:g.29708924A= , CM000684.1:g.29708924A= GRCh37
NC_000022.9:g.28038924A= NCBI36
NG_032959.1:g.10929A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*366T= MANE Select ENSP00000216101.6:n.*366T=
ENST00000216101.6:c.*366T= ENSP00000216101.6:n.*366T=
ENST00000401450.3:c.*924T= ENSP00000386095.3:n.*924T=
NM_006477.4:c.*366T= NP_006468.1:n.*366T=
XM_011529821.1:c.*366T= XP_011528123.1:n.*366T=
XM_011529822.1:c.*366T= XP_011528124.1:n.*366T=
XM_011529823.1:c.*366T= XP_011528125.1:n.*366T=
NM_006477.5:c.*366T= MANE Select NP_006468.1:n.*366T=