Canonical Allele Identifier: CA2400518774
Gene: RASL10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313179C= , CM000684.2:g.29313179C= GRCh38
NC_000022.10:g.29709168C= , CM000684.1:g.29709168C= GRCh37
NC_000022.9:g.28039168C= NCBI36
NG_032959.1:g.11173C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*122G= MANE Select ENSP00000216101.6:n.*122G=
ENST00000216101.6:c.*122G= ENSP00000216101.6:n.*122G=
ENST00000401450.3:c.*680G= ENSP00000386095.3:n.*680G=
NM_006477.4:c.*122G= NP_006468.1:n.*122G=
XM_011529821.1:c.*122G= XP_011528123.1:n.*122G=
XM_011529822.1:c.*122G= XP_011528124.1:n.*122G=
XM_011529823.1:c.*122G= XP_011528125.1:n.*122G=
NM_006477.5:c.*122G= MANE Select NP_006468.1:n.*122G=
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