Canonical Allele Identifier: CA752236874
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs1205267389
gnomAD v3: 22-29312988-C-T
gnomAD v4: 22-29312988-C-T
MyVariant Identifiers: chr22:g.29708977C>T (hg19) chr22:g.29312988C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29312988C>T , CM000684.2:g.29312988C>T GRCh38
NC_000022.10:g.29708977C>T , CM000684.1:g.29708977C>T GRCh37
NC_000022.9:g.28038977C>T NCBI36
NG_032959.1:g.10982C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*313G>A MANE Select ENSP00000216101.6:n.*313G>A
ENST00000216101.6:c.*313G>A ENSP00000216101.6:n.*313G>A
ENST00000401450.3:c.*871G>A ENSP00000386095.3:n.*871G>A
NM_006477.4:c.*313G>A NP_006468.1:n.*313G>A
XM_011529821.1:c.*313G>A XP_011528123.1:n.*313G>A
XM_011529822.1:c.*313G>A XP_011528124.1:n.*313G>A
XM_011529823.1:c.*313G>A XP_011528125.1:n.*313G>A
NM_006477.5:c.*313G>A MANE Select NP_006468.1:n.*313G>A
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