Canonical Allele Identifier: CA2655998219
Gene: RASL10A HGNC NCBI

Linked Data

gnomAD v4: 22-29313170-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313170A>G , CM000684.2:g.29313170A>G GRCh38
NC_000022.10:g.29709159A>G , CM000684.1:g.29709159A>G GRCh37
NC_000022.9:g.28039159A>G NCBI36
NG_032959.1:g.11164A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*131T>C MANE Select ENSP00000216101.6:n.*131T>C
ENST00000216101.6:c.*131T>C ENSP00000216101.6:n.*131T>C
ENST00000401450.3:c.*689T>C ENSP00000386095.3:n.*689T>C
NM_006477.4:c.*131T>C NP_006468.1:n.*131T>C
XM_011529821.1:c.*131T>C XP_011528123.1:n.*131T>C
XM_011529822.1:c.*131T>C XP_011528124.1:n.*131T>C
XM_011529823.1:c.*131T>C XP_011528125.1:n.*131T>C
NM_006477.5:c.*131T>C MANE Select NP_006468.1:n.*131T>C
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