Canonical Allele Identifier: CA2400518802
Gene: RASL10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313230T= , CM000684.2:g.29313230T= GRCh38
NC_000022.10:g.29709219T= , CM000684.1:g.29709219T= GRCh37
NC_000022.9:g.28039219T= NCBI36
NG_032959.1:g.11224T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*71A= MANE Select ENSP00000216101.6:n.*71A=
ENST00000216101.6:c.*71A= ENSP00000216101.6:n.*71A=
ENST00000401450.3:c.*629A= ENSP00000386095.3:n.*629A=
NM_006477.4:c.*71A= NP_006468.1:n.*71A=
XM_011529821.1:c.*71A= XP_011528123.1:n.*71A=
XM_011529822.1:c.*71A= XP_011528124.1:n.*71A=
XM_011529823.1:c.*71A= XP_011528125.1:n.*71A=
NM_006477.5:c.*71A= MANE Select NP_006468.1:n.*71A=