Canonical Allele Identifier: CA2655997871
Gene: RASL10A HGNC NCBI

Linked Data

gnomAD v4: 22-29312936-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29312936A>C , CM000684.2:g.29312936A>C GRCh38
NC_000022.10:g.29708925A>C , CM000684.1:g.29708925A>C GRCh37
NC_000022.9:g.28038925A>C NCBI36
NG_032959.1:g.10930A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*365T>G MANE Select ENSP00000216101.6:n.*365T>G
ENST00000216101.6:c.*365T>G ENSP00000216101.6:n.*365T>G
ENST00000401450.3:c.*923T>G ENSP00000386095.3:n.*923T>G
NM_006477.4:c.*365T>G NP_006468.1:n.*365T>G
XM_011529821.1:c.*365T>G XP_011528123.1:n.*365T>G
XM_011529822.1:c.*365T>G XP_011528124.1:n.*365T>G
XM_011529823.1:c.*365T>G XP_011528125.1:n.*365T>G
NM_006477.5:c.*365T>G MANE Select NP_006468.1:n.*365T>G
Search 100 bp 5'
Search 100 bp 3'