Canonical Allele Identifier: CA638822436
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs1192387811
gnomAD v2: 22-29709059-T-G
gnomAD v3: 22-29313070-T-G
gnomAD v4: 22-29313070-T-G
MyVariant Identifiers: chr22:g.29709059T>G (hg19) chr22:g.29313070T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313070T>G , CM000684.2:g.29313070T>G GRCh38
NC_000022.10:g.29709059T>G , CM000684.1:g.29709059T>G GRCh37
NC_000022.9:g.28039059T>G NCBI36
NG_032959.1:g.11064T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*231A>C MANE Select ENSP00000216101.6:n.*231A>C
ENST00000216101.6:c.*231A>C ENSP00000216101.6:n.*231A>C
ENST00000401450.3:c.*789A>C ENSP00000386095.3:n.*789A>C
NM_006477.4:c.*231A>C NP_006468.1:n.*231A>C
XM_011529821.1:c.*231A>C XP_011528123.1:n.*231A>C
XM_011529822.1:c.*231A>C XP_011528124.1:n.*231A>C
XM_011529823.1:c.*231A>C XP_011528125.1:n.*231A>C
NM_006477.5:c.*231A>C MANE Select NP_006468.1:n.*231A>C
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