Canonical Allele Identifier: CA638954940
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs1431548775
gnomAD v2: 22-29709247-C-G
gnomAD v4: 22-29313258-C-G
MyVariant Identifiers: chr22:g.29709247C>G (hg19) chr22:g.29313258C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313258C>G , CM000684.2:g.29313258C>G GRCh38
NC_000022.10:g.29709247C>G , CM000684.1:g.29709247C>G GRCh37
NC_000022.9:g.28039247C>G NCBI36
NG_032959.1:g.11252C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*43G>C MANE Select ENSP00000216101.6:n.*43G>C
ENST00000216101.6:c.*43G>C ENSP00000216101.6:n.*43G>C
ENST00000401450.3:c.*601G>C ENSP00000386095.3:n.*601G>C
NM_006477.4:c.*43G>C NP_006468.1:n.*43G>C
XM_011529821.1:c.*43G>C XP_011528123.1:n.*43G>C
XM_011529822.1:c.*43G>C XP_011528124.1:n.*43G>C
XM_011529823.1:c.*43G>C XP_011528125.1:n.*43G>C
NM_006477.5:c.*43G>C MANE Select NP_006468.1:n.*43G>C
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