Canonical Allele Identifier: CA2400518818
Gene: RASL10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313252_29313253delinsAT , CM000684.2:g.29313252_29313253delinsAT GRCh38
NC_000022.10:g.29709241_29709242delinsAT , CM000684.1:g.29709241_29709242delinsAT GRCh37
NC_000022.9:g.28039241_28039242delinsAT NCBI36
NG_032959.1:g.11246_11247delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*48_*49delinsAT MANE Select ENSP00000216101.6:n.*48_*49delinsAT
ENST00000216101.6:c.*48_*49delinsAT ENSP00000216101.6:n.*48_*49delinsAT
ENST00000401450.3:c.*606_*607delinsAT ENSP00000386095.3:n.*606_*607delinsAT
NM_006477.4:c.*48_*49delinsAT NP_006468.1:n.*48_*49delinsAT
XM_011529821.1:c.*48_*49delinsAT XP_011528123.1:n.*48_*49delinsAT
XM_011529822.1:c.*48_*49delinsAT XP_011528124.1:n.*48_*49delinsAT
XM_011529823.1:c.*48_*49delinsAT XP_011528125.1:n.*48_*49delinsAT
NM_006477.5:c.*48_*49delinsAT MANE Select NP_006468.1:n.*48_*49delinsAT