Canonical Allele Identifier: CA1024911895
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs2061427554

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313003_29313006dup , CM000684.2:g.29313003_29313006dup GRCh38
NC_000022.10:g.29708992_29708995dup , CM000684.1:g.29708992_29708995dup GRCh37
NC_000022.9:g.28038992_28038995dup NCBI36
NG_032959.1:g.10997_11000dup

Transcript Alleles

HGVS Amino-acid change
ENST00000216101.7:c.*295_*298dup MANE Select ENSP00000216101.6:n.*295_*298dup
ENST00000216101.6:c.*295_*298dup ENSP00000216101.6:n.*295_*298dup
ENST00000401450.3:c.*853_*856dup ENSP00000386095.3:n.*853_*856dup
NM_006477.4:c.*295_*298dup NP_006468.1:n.*295_*298dup
XM_011529821.1:c.*295_*298dup XP_011528123.1:n.*295_*298dup
XM_011529822.1:c.*295_*298dup XP_011528124.1:n.*295_*298dup
XM_011529823.1:c.*295_*298dup XP_011528125.1:n.*295_*298dup
NM_006477.5:c.*295_*298dup MANE Select NP_006468.1:n.*295_*298dup