Canonical Allele Identifier: CA2655998150
Gene: RASL10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313122G>A , CM000684.2:g.29313122G>A GRCh38
NC_000022.10:g.29709111G>A , CM000684.1:g.29709111G>A GRCh37
NC_000022.9:g.28039111G>A NCBI36
NG_032959.1:g.11116G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000216101.7:c.*179C>T MANE Select ENSP00000216101.6:n.*179C>T
ENST00000216101.6:c.*179C>T ENSP00000216101.6:n.*179C>T
ENST00000401450.3:c.*737C>T ENSP00000386095.3:n.*737C>T
NM_006477.4:c.*179C>T NP_006468.1:n.*179C>T
XM_011529821.1:c.*179C>T XP_011528123.1:n.*179C>T
XM_011529822.1:c.*179C>T XP_011528124.1:n.*179C>T
XM_011529823.1:c.*179C>T XP_011528125.1:n.*179C>T
NM_006477.5:c.*179C>T MANE Select NP_006468.1:n.*179C>T