Canonical Allele Identifier: CA323103370

Gene: RASL10A

Linked Data

• dbSNP Id: rs998976592
• gnomAD v3: 22-29313154-TAGG-T
• gnomAD v4: 22-29313154-TAGG-T
• MyVariant Identifiers: chr22:g.29709144_29709146del (hg19) ; chr22:g.29313155_29313157del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313157_29313159del , CM000684.2:g.29313157_29313159del	GRCh38
NC_000022.10:g.29709146_29709148del , CM000684.1:g.29709146_29709148del	GRCh37
NC_000022.9:g.28039146_28039148del	NCBI36
NG_032959.1:g.11151_11153del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216101.7:c.*144_*146del MANE Select	ENSP00000216101.6:n.*144_*146del
ENST00000216101.6:c.*144_*146del	ENSP00000216101.6:n.*144_*146del
ENST00000401450.3:c.*702_*704del	ENSP00000386095.3:n.*702_*704del
NM_006477.4:c.*144_*146del	NP_006468.1:n.*144_*146del
XM_011529821.1:c.*144_*146del	XP_011528123.1:n.*144_*146del
XM_011529822.1:c.*144_*146del	XP_011528124.1:n.*144_*146del
XM_011529823.1:c.*144_*146del	XP_011528125.1:n.*144_*146del
NM_006477.5:c.*144_*146del MANE Select	NP_006468.1:n.*144_*146del