Canonical Allele Identifier: CA2655998243
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs1316290608
gnomAD v4: 22-29313200-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313200T>G , CM000684.2:g.29313200T>G GRCh38
NC_000022.10:g.29709189T>G , CM000684.1:g.29709189T>G GRCh37
NC_000022.9:g.28039189T>G NCBI36
NG_032959.1:g.11194T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*101A>C MANE Select ENSP00000216101.6:n.*101A>C
ENST00000216101.6:c.*101A>C ENSP00000216101.6:n.*101A>C
ENST00000401450.3:c.*659A>C ENSP00000386095.3:n.*659A>C
NM_006477.4:c.*101A>C NP_006468.1:n.*101A>C
XM_011529821.1:c.*101A>C XP_011528123.1:n.*101A>C
XM_011529822.1:c.*101A>C XP_011528124.1:n.*101A>C
XM_011529823.1:c.*101A>C XP_011528125.1:n.*101A>C
NM_006477.5:c.*101A>C MANE Select NP_006468.1:n.*101A>C
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