Canonical Allele Identifier: CA2400518751

Gene: RASL10A

Linked Data

• dbSNP Id: rs2061428520

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313141_29313148del , CM000684.2:g.29313141_29313148del	GRCh38
NC_000022.10:g.29709130_29709137del , CM000684.1:g.29709130_29709137del	GRCh37
NC_000022.9:g.28039130_28039137del	NCBI36
NG_032959.1:g.11135_11142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216101.7:c.*155_*162del MANE Select	ENSP00000216101.6:n.*155_*162del
ENST00000216101.6:c.*155_*162del	ENSP00000216101.6:n.*155_*162del
ENST00000401450.3:c.*713_*720del	ENSP00000386095.3:n.*713_*720del
NM_006477.4:c.*155_*162del	NP_006468.1:n.*155_*162del
XM_011529821.1:c.*155_*162del	XP_011528123.1:n.*155_*162del
XM_011529822.1:c.*155_*162del	XP_011528124.1:n.*155_*162del
XM_011529823.1:c.*155_*162del	XP_011528125.1:n.*155_*162del
NM_006477.5:c.*155_*162del MANE Select	NP_006468.1:n.*155_*162del