Canonical Allele Identifier: CA2400518752

Gene: RASL10A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313139_29313140delinsAG , CM000684.2:g.29313139_29313140delinsAG	GRCh38
NC_000022.10:g.29709128_29709129delinsAG , CM000684.1:g.29709128_29709129delinsAG	GRCh37
NC_000022.9:g.28039128_28039129delinsAG	NCBI36
NG_032959.1:g.11133_11134delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216101.7:c.*161_*162delinsCT MANE Select	ENSP00000216101.6:n.*161_*162delinsCT
ENST00000216101.6:c.*161_*162delinsCT	ENSP00000216101.6:n.*161_*162delinsCT
ENST00000401450.3:c.*719_*720delinsCT	ENSP00000386095.3:n.*719_*720delinsCT
NM_006477.4:c.*161_*162delinsCT	NP_006468.1:n.*161_*162delinsCT
XM_011529821.1:c.*161_*162delinsCT	XP_011528123.1:n.*161_*162delinsCT
XM_011529822.1:c.*161_*162delinsCT	XP_011528124.1:n.*161_*162delinsCT
XM_011529823.1:c.*161_*162delinsCT	XP_011528125.1:n.*161_*162delinsCT
NM_006477.5:c.*161_*162delinsCT MANE Select	NP_006468.1:n.*161_*162delinsCT