Canonical Allele Identifier: CA2400518754
Gene: RASL10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313144G= , CM000684.2:g.29313144G= GRCh38
NC_000022.10:g.29709133G= , CM000684.1:g.29709133G= GRCh37
NC_000022.9:g.28039133G= NCBI36
NG_032959.1:g.11138G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*157C= MANE Select ENSP00000216101.6:n.*157C=
ENST00000216101.6:c.*157C= ENSP00000216101.6:n.*157C=
ENST00000401450.3:c.*715C= ENSP00000386095.3:n.*715C=
NM_006477.4:c.*157C= NP_006468.1:n.*157C=
XM_011529821.1:c.*157C= XP_011528123.1:n.*157C=
XM_011529822.1:c.*157C= XP_011528124.1:n.*157C=
XM_011529823.1:c.*157C= XP_011528125.1:n.*157C=
NM_006477.5:c.*157C= MANE Select NP_006468.1:n.*157C=