Canonical Allele Identifier: CA2400518827
Gene: RASL10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313263C= , CM000684.2:g.29313263C= GRCh38
NC_000022.10:g.29709252C= , CM000684.1:g.29709252C= GRCh37
NC_000022.9:g.28039252C= NCBI36
NG_032959.1:g.11257C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*38G= MANE Select ENSP00000216101.6:n.*38G=
ENST00000216101.6:c.*38G= ENSP00000216101.6:n.*38G=
ENST00000401450.3:c.*596G= ENSP00000386095.3:n.*596G=
NM_006477.4:c.*38G= NP_006468.1:n.*38G=
XM_011529821.1:c.*38G= XP_011528123.1:n.*38G=
XM_011529822.1:c.*38G= XP_011528124.1:n.*38G=
XM_011529823.1:c.*38G= XP_011528125.1:n.*38G=
NM_006477.5:c.*38G= MANE Select NP_006468.1:n.*38G=
Search 100 bp 5'
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