Canonical Allele Identifier: CA1024911932
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs2061428137
gnomAD v3: 22-29313085-G-T
gnomAD v4: 22-29313085-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313085G>T , CM000684.2:g.29313085G>T GRCh38
NC_000022.10:g.29709074G>T , CM000684.1:g.29709074G>T GRCh37
NC_000022.9:g.28039074G>T NCBI36
NG_032959.1:g.11079G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*216C>A MANE Select ENSP00000216101.6:n.*216C>A
ENST00000216101.6:c.*216C>A ENSP00000216101.6:n.*216C>A
ENST00000401450.3:c.*774C>A ENSP00000386095.3:n.*774C>A
NM_006477.4:c.*216C>A NP_006468.1:n.*216C>A
XM_011529821.1:c.*216C>A XP_011528123.1:n.*216C>A
XM_011529822.1:c.*216C>A XP_011528124.1:n.*216C>A
XM_011529823.1:c.*216C>A XP_011528125.1:n.*216C>A
NM_006477.5:c.*216C>A MANE Select NP_006468.1:n.*216C>A
Search 100 bp 5'
Search 100 bp 3'