Canonical Allele Identifier: CA2400518689

Gene: RASL10A

Linked Data

• dbSNP Id: rs2061427584

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313005_29313007del , CM000684.2:g.29313005_29313007del	GRCh38
NC_000022.10:g.29708994_29708996del , CM000684.1:g.29708994_29708996del	GRCh37
NC_000022.9:g.28038994_28038996del	NCBI36
NG_032959.1:g.10999_11001del

Transcript Alleles

HGVS	Amino-acid change
ENST00000216101.7:c.*296_*298del MANE Select	ENSP00000216101.6:n.*296_*298del
ENST00000216101.6:c.*296_*298del	ENSP00000216101.6:n.*296_*298del
ENST00000401450.3:c.*854_*856del	ENSP00000386095.3:n.*854_*856del
NM_006477.4:c.*296_*298del	NP_006468.1:n.*296_*298del
XM_011529821.1:c.*296_*298del	XP_011528123.1:n.*296_*298del
XM_011529822.1:c.*296_*298del	XP_011528124.1:n.*296_*298del
XM_011529823.1:c.*296_*298del	XP_011528125.1:n.*296_*298del
NM_006477.5:c.*296_*298del MANE Select	NP_006468.1:n.*296_*298del