Canonical Allele Identifier: CA638954935
Gene: RASL10A HGNC NCBI

Linked Data

dbSNP Id: rs1274816617
gnomAD v2: 22-29709224-T-A
gnomAD v3: 22-29313235-T-A
gnomAD v4: 22-29313235-T-A
MyVariant Identifiers: chr22:g.29709224T>A (hg19) chr22:g.29313235T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313235T>A , CM000684.2:g.29313235T>A GRCh38
NC_000022.10:g.29709224T>A , CM000684.1:g.29709224T>A GRCh37
NC_000022.9:g.28039224T>A NCBI36
NG_032959.1:g.11229T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*66A>T MANE Select ENSP00000216101.6:n.*66A>T
ENST00000216101.6:c.*66A>T ENSP00000216101.6:n.*66A>T
ENST00000401450.3:c.*624A>T ENSP00000386095.3:n.*624A>T
NM_006477.4:c.*66A>T NP_006468.1:n.*66A>T
XM_011529821.1:c.*66A>T XP_011528123.1:n.*66A>T
XM_011529822.1:c.*66A>T XP_011528124.1:n.*66A>T
XM_011529823.1:c.*66A>T XP_011528125.1:n.*66A>T
NM_006477.5:c.*66A>T MANE Select NP_006468.1:n.*66A>T
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