Canonical Allele Identifier: CA2400518746
Gene: RASL10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313127A= , CM000684.2:g.29313127A= GRCh38
NC_000022.10:g.29709116A= , CM000684.1:g.29709116A= GRCh37
NC_000022.9:g.28039116A= NCBI36
NG_032959.1:g.11121A=

Transcript Alleles

HGVS Amino-acid change
ENST00000216101.7:c.*174T= MANE Select ENSP00000216101.6:n.*174T=
ENST00000216101.6:c.*174T= ENSP00000216101.6:n.*174T=
ENST00000401450.3:c.*732T= ENSP00000386095.3:n.*732T=
NM_006477.4:c.*174T= NP_006468.1:n.*174T=
XM_011529821.1:c.*174T= XP_011528123.1:n.*174T=
XM_011529822.1:c.*174T= XP_011528124.1:n.*174T=
XM_011529823.1:c.*174T= XP_011528125.1:n.*174T=
NM_006477.5:c.*174T= MANE Select NP_006468.1:n.*174T=