Canonical Allele Identifier: CA752236927
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs1275393060
gnomAD v3: 22-29313123-T-TC
gnomAD v4: 22-29313123-T-TC
MyVariant Identifiers: chr22:g.29709112_29709113insC (hg19) chr22:g.29313123_29313124insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313125dup , CM000684.2:g.29313125dup GRCh38
NC_000022.10:g.29709114dup , CM000684.1:g.29709114dup GRCh37
NC_000022.9:g.28039114dup NCBI36
NG_032959.1:g.11119dup

Transcript Alleles

HGVS Amino-acid change
ENST00000216101.7:c.*177dup MANE Select ENSP00000216101.6:n.*177dup
ENST00000216101.6:c.*177dup ENSP00000216101.6:n.*177dup
ENST00000401450.3:c.*735dup ENSP00000386095.3:n.*735dup
NM_006477.4:c.*177dup NP_006468.1:n.*177dup
XM_011529821.1:c.*177dup XP_011528123.1:n.*177dup
XM_011529822.1:c.*177dup XP_011528124.1:n.*177dup
XM_011529823.1:c.*177dup XP_011528125.1:n.*177dup
NM_006477.5:c.*177dup MANE Select NP_006468.1:n.*177dup
Search 100 bp 5'
Search 100 bp 3'