Canonical Allele Identifier: CA2655998179
Gene: RASL10A HGNC NCBI

Linked Data

gnomAD v4: 22-29313139-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313139A>G , CM000684.2:g.29313139A>G GRCh38
NC_000022.10:g.29709128A>G , CM000684.1:g.29709128A>G GRCh37
NC_000022.9:g.28039128A>G NCBI36
NG_032959.1:g.11133A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*162T>C MANE Select ENSP00000216101.6:n.*162T>C
ENST00000216101.6:c.*162T>C ENSP00000216101.6:n.*162T>C
ENST00000401450.3:c.*720T>C ENSP00000386095.3:n.*720T>C
NM_006477.4:c.*162T>C NP_006468.1:n.*162T>C
XM_011529821.1:c.*162T>C XP_011528123.1:n.*162T>C
XM_011529822.1:c.*162T>C XP_011528124.1:n.*162T>C
XM_011529823.1:c.*162T>C XP_011528125.1:n.*162T>C
NM_006477.5:c.*162T>C MANE Select NP_006468.1:n.*162T>C
Search 100 bp 5'
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