Canonical Allele Identifier: CA2655998237
Gene: RASL10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313193G>A , CM000684.2:g.29313193G>A GRCh38
NC_000022.10:g.29709182G>A , CM000684.1:g.29709182G>A GRCh37
NC_000022.9:g.28039182G>A NCBI36
NG_032959.1:g.11187G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*108C>T MANE Select ENSP00000216101.6:n.*108C>T
ENST00000216101.6:c.*108C>T ENSP00000216101.6:n.*108C>T
ENST00000401450.3:c.*666C>T ENSP00000386095.3:n.*666C>T
NM_006477.4:c.*108C>T NP_006468.1:n.*108C>T
XM_011529821.1:c.*108C>T XP_011528123.1:n.*108C>T
XM_011529822.1:c.*108C>T XP_011528124.1:n.*108C>T
XM_011529823.1:c.*108C>T XP_011528125.1:n.*108C>T
NM_006477.5:c.*108C>T MANE Select NP_006468.1:n.*108C>T