Canonical Allele Identifier: CA2400518656
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs1177556348

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29312947C>G , CM000684.2:g.29312947C>G GRCh38
NC_000022.10:g.29708936C>G , CM000684.1:g.29708936C>G GRCh37
NC_000022.9:g.28038936C>G NCBI36
NG_032959.1:g.10941C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*354G>C MANE Select ENSP00000216101.6:n.*354G>C
ENST00000216101.6:c.*354G>C ENSP00000216101.6:n.*354G>C
ENST00000401450.3:c.*912G>C ENSP00000386095.3:n.*912G>C
NM_006477.4:c.*354G>C NP_006468.1:n.*354G>C
XM_011529821.1:c.*354G>C XP_011528123.1:n.*354G>C
XM_011529822.1:c.*354G>C XP_011528124.1:n.*354G>C
XM_011529823.1:c.*354G>C XP_011528125.1:n.*354G>C
NM_006477.5:c.*354G>C MANE Select NP_006468.1:n.*354G>C