Canonical Allele Identifier: CA2655998230
Gene: RASL10A HGNC NCBI

Linked Data

gnomAD v4: 22-29313185-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313185A>G , CM000684.2:g.29313185A>G GRCh38
NC_000022.10:g.29709174A>G , CM000684.1:g.29709174A>G GRCh37
NC_000022.9:g.28039174A>G NCBI36
NG_032959.1:g.11179A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*116T>C MANE Select ENSP00000216101.6:n.*116T>C
ENST00000216101.6:c.*116T>C ENSP00000216101.6:n.*116T>C
ENST00000401450.3:c.*674T>C ENSP00000386095.3:n.*674T>C
NM_006477.4:c.*116T>C NP_006468.1:n.*116T>C
XM_011529821.1:c.*116T>C XP_011528123.1:n.*116T>C
XM_011529822.1:c.*116T>C XP_011528124.1:n.*116T>C
XM_011529823.1:c.*116T>C XP_011528125.1:n.*116T>C
NM_006477.5:c.*116T>C MANE Select NP_006468.1:n.*116T>C
Search 100 bp 5'
Search 100 bp 3'