Canonical Allele Identifier: CA638954938
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs1424276467
gnomAD v2: 22-29709240-G-C
gnomAD v3: 22-29313251-G-C
gnomAD v4: 22-29313251-G-C
MyVariant Identifiers: chr22:g.29709240G>C (hg19) chr22:g.29313251G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313251G>C , CM000684.2:g.29313251G>C GRCh38
NC_000022.10:g.29709240G>C , CM000684.1:g.29709240G>C GRCh37
NC_000022.9:g.28039240G>C NCBI36
NG_032959.1:g.11245G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*50C>G MANE Select ENSP00000216101.6:n.*50C>G
ENST00000216101.6:c.*50C>G ENSP00000216101.6:n.*50C>G
ENST00000401450.3:c.*608C>G ENSP00000386095.3:n.*608C>G
NM_006477.4:c.*50C>G NP_006468.1:n.*50C>G
XM_011529821.1:c.*50C>G XP_011528123.1:n.*50C>G
XM_011529822.1:c.*50C>G XP_011528124.1:n.*50C>G
XM_011529823.1:c.*50C>G XP_011528125.1:n.*50C>G
NM_006477.5:c.*50C>G MANE Select NP_006468.1:n.*50C>G
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