Canonical Allele Identifier: CA2655998120
Gene: RASL10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313110G>C , CM000684.2:g.29313110G>C GRCh38
NC_000022.10:g.29709099G>C , CM000684.1:g.29709099G>C GRCh37
NC_000022.9:g.28039099G>C NCBI36
NG_032959.1:g.11104G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216101.7:c.*191C>G MANE Select ENSP00000216101.6:n.*191C>G
ENST00000216101.6:c.*191C>G ENSP00000216101.6:n.*191C>G
ENST00000401450.3:c.*749C>G ENSP00000386095.3:n.*749C>G
NM_006477.4:c.*191C>G NP_006468.1:n.*191C>G
XM_011529821.1:c.*191C>G XP_011528123.1:n.*191C>G
XM_011529822.1:c.*191C>G XP_011528124.1:n.*191C>G
XM_011529823.1:c.*191C>G XP_011528125.1:n.*191C>G
NM_006477.5:c.*191C>G MANE Select NP_006468.1:n.*191C>G