Canonical Allele Identifier: CA2400518726
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs2061428060

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313073G>A , CM000684.2:g.29313073G>A GRCh38
NC_000022.10:g.29709062G>A , CM000684.1:g.29709062G>A GRCh37
NC_000022.9:g.28039062G>A NCBI36
NG_032959.1:g.11067G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*228C>T MANE Select ENSP00000216101.6:n.*228C>T
ENST00000216101.6:c.*228C>T ENSP00000216101.6:n.*228C>T
ENST00000401450.3:c.*786C>T ENSP00000386095.3:n.*786C>T
NM_006477.4:c.*228C>T NP_006468.1:n.*228C>T
XM_011529821.1:c.*228C>T XP_011528123.1:n.*228C>T
XM_011529822.1:c.*228C>T XP_011528124.1:n.*228C>T
XM_011529823.1:c.*228C>T XP_011528125.1:n.*228C>T
NM_006477.5:c.*228C>T MANE Select NP_006468.1:n.*228C>T