Canonical Allele Identifier: CA2400518767
Gene: RASL10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313169G= , CM000684.2:g.29313169G= GRCh38
NC_000022.10:g.29709158G= , CM000684.1:g.29709158G= GRCh37
NC_000022.9:g.28039158G= NCBI36
NG_032959.1:g.11163G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*132C= MANE Select ENSP00000216101.6:n.*132C=
ENST00000216101.6:c.*132C= ENSP00000216101.6:n.*132C=
ENST00000401450.3:c.*690C= ENSP00000386095.3:n.*690C=
NM_006477.4:c.*132C= NP_006468.1:n.*132C=
XM_011529821.1:c.*132C= XP_011528123.1:n.*132C=
XM_011529822.1:c.*132C= XP_011528124.1:n.*132C=
XM_011529823.1:c.*132C= XP_011528125.1:n.*132C=
NM_006477.5:c.*132C= MANE Select NP_006468.1:n.*132C=
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