Canonical Allele Identifier: CA1024911958

Gene: RASL10A

Linked Data

• dbSNP Id: rs2061428610
• gnomAD v3: 22-29313144-G-GC
• gnomAD v4: 22-29313144-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313146dup , CM000684.2:g.29313146dup	GRCh38
NC_000022.10:g.29709135dup , CM000684.1:g.29709135dup	GRCh37
NC_000022.9:g.28039135dup	NCBI36
NG_032959.1:g.11140dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216101.7:c.*156dup MANE Select	ENSP00000216101.6:n.*156dup
ENST00000216101.6:c.*156dup	ENSP00000216101.6:n.*156dup
ENST00000401450.3:c.*714dup	ENSP00000386095.3:n.*714dup
NM_006477.4:c.*156dup	NP_006468.1:n.*156dup
XM_011529821.1:c.*156dup	XP_011528123.1:n.*156dup
XM_011529822.1:c.*156dup	XP_011528124.1:n.*156dup
XM_011529823.1:c.*156dup	XP_011528125.1:n.*156dup
NM_006477.5:c.*156dup MANE Select	NP_006468.1:n.*156dup