Canonical Allele Identifier: CA2655998194

Gene: RASL10A

Linked Data

• gnomAD v4: 22-29313145-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313145C>A , CM000684.2:g.29313145C>A	GRCh38
NC_000022.10:g.29709134C>A , CM000684.1:g.29709134C>A	GRCh37
NC_000022.9:g.28039134C>A	NCBI36
NG_032959.1:g.11139C>A

Transcript Alleles

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