Canonical Allele Identifier: CA2400518762
Gene: RASL10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313154_29313157delinsTAGG , CM000684.2:g.29313154_29313157delinsTAGG GRCh38
NC_000022.10:g.29709143_29709146delinsTAGG , CM000684.1:g.29709143_29709146delinsTAGG GRCh37
NC_000022.9:g.28039143_28039146delinsTAGG NCBI36
NG_032959.1:g.11148_11151delinsTAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*144_*147delinsCCTA MANE Select ENSP00000216101.6:n.*144_*147delinsCCTA
ENST00000216101.6:c.*144_*147delinsCCTA ENSP00000216101.6:n.*144_*147delinsCCTA
ENST00000401450.3:c.*702_*705delinsCCTA ENSP00000386095.3:n.*702_*705delinsCCTA
NM_006477.4:c.*144_*147delinsCCTA NP_006468.1:n.*144_*147delinsCCTA
XM_011529821.1:c.*144_*147delinsCCTA XP_011528123.1:n.*144_*147delinsCCTA
XM_011529822.1:c.*144_*147delinsCCTA XP_011528124.1:n.*144_*147delinsCCTA
XM_011529823.1:c.*144_*147delinsCCTA XP_011528125.1:n.*144_*147delinsCCTA
NM_006477.5:c.*144_*147delinsCCTA MANE Select NP_006468.1:n.*144_*147delinsCCTA