Canonical Allele Identifier: CA752236921
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs1204984428
gnomAD v3: 22-29313113-C-T
gnomAD v4: 22-29313113-C-T
MyVariant Identifiers: chr22:g.29709102C>T (hg19) chr22:g.29313113C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313113C>T , CM000684.2:g.29313113C>T GRCh38
NC_000022.10:g.29709102C>T , CM000684.1:g.29709102C>T GRCh37
NC_000022.9:g.28039102C>T NCBI36
NG_032959.1:g.11107C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000216101.7:c.*188G>A MANE Select ENSP00000216101.6:n.*188G>A
ENST00000216101.6:c.*188G>A ENSP00000216101.6:n.*188G>A
ENST00000401450.3:c.*746G>A ENSP00000386095.3:n.*746G>A
NM_006477.4:c.*188G>A NP_006468.1:n.*188G>A
XM_011529821.1:c.*188G>A XP_011528123.1:n.*188G>A
XM_011529822.1:c.*188G>A XP_011528124.1:n.*188G>A
XM_011529823.1:c.*188G>A XP_011528125.1:n.*188G>A
NM_006477.5:c.*188G>A MANE Select NP_006468.1:n.*188G>A
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