Canonical Allele Identifier: CA2400518816
Gene: RASL10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313250T= , CM000684.2:g.29313250T= GRCh38
NC_000022.10:g.29709239T= , CM000684.1:g.29709239T= GRCh37
NC_000022.9:g.28039239T= NCBI36
NG_032959.1:g.11244T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*51A= MANE Select ENSP00000216101.6:n.*51A=
ENST00000216101.6:c.*51A= ENSP00000216101.6:n.*51A=
ENST00000401450.3:c.*609A= ENSP00000386095.3:n.*609A=
NM_006477.4:c.*51A= NP_006468.1:n.*51A=
XM_011529821.1:c.*51A= XP_011528123.1:n.*51A=
XM_011529822.1:c.*51A= XP_011528124.1:n.*51A=
XM_011529823.1:c.*51A= XP_011528125.1:n.*51A=
NM_006477.5:c.*51A= MANE Select NP_006468.1:n.*51A=
Search 100 bp 5'
Search 100 bp 3'