Canonical Allele Identifier: CA2655998160
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs2061428462
gnomAD v4: 22-29313128-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313128T>G , CM000684.2:g.29313128T>G GRCh38
NC_000022.10:g.29709117T>G , CM000684.1:g.29709117T>G GRCh37
NC_000022.9:g.28039117T>G NCBI36
NG_032959.1:g.11122T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000216101.7:c.*173A>C MANE Select ENSP00000216101.6:n.*173A>C
ENST00000216101.6:c.*173A>C ENSP00000216101.6:n.*173A>C
ENST00000401450.3:c.*731A>C ENSP00000386095.3:n.*731A>C
NM_006477.4:c.*173A>C NP_006468.1:n.*173A>C
XM_011529821.1:c.*173A>C XP_011528123.1:n.*173A>C
XM_011529822.1:c.*173A>C XP_011528124.1:n.*173A>C
XM_011529823.1:c.*173A>C XP_011528125.1:n.*173A>C
NM_006477.5:c.*173A>C MANE Select NP_006468.1:n.*173A>C
Search 100 bp 5'
Search 100 bp 3'