Canonical Allele Identifier: CA2400518794
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs2061429168
gnomAD v4: 22-29313217-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313217T>G , CM000684.2:g.29313217T>G GRCh38
NC_000022.10:g.29709206T>G , CM000684.1:g.29709206T>G GRCh37
NC_000022.9:g.28039206T>G NCBI36
NG_032959.1:g.11211T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*84A>C MANE Select ENSP00000216101.6:n.*84A>C
ENST00000216101.6:c.*84A>C ENSP00000216101.6:n.*84A>C
ENST00000401450.3:c.*642A>C ENSP00000386095.3:n.*642A>C
NM_006477.4:c.*84A>C NP_006468.1:n.*84A>C
XM_011529821.1:c.*84A>C XP_011528123.1:n.*84A>C
XM_011529822.1:c.*84A>C XP_011528124.1:n.*84A>C
XM_011529823.1:c.*84A>C XP_011528125.1:n.*84A>C
NM_006477.5:c.*84A>C MANE Select NP_006468.1:n.*84A>C
Search 100 bp 5'
Search 100 bp 3'