Canonical Allele Identifier: CA2400518649

Gene: RASL10A

Linked Data

• dbSNP Id: rs1602659392

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29312939T>C , CM000684.2:g.29312939T>C	GRCh38
NC_000022.10:g.29708928T>C , CM000684.1:g.29708928T>C	GRCh37
NC_000022.9:g.28038928T>C	NCBI36
NG_032959.1:g.10933T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216101.7:c.*362A>G MANE Select	ENSP00000216101.6:n.*362A>G
ENST00000216101.6:c.*362A>G	ENSP00000216101.6:n.*362A>G
ENST00000401450.3:c.*920A>G	ENSP00000386095.3:n.*920A>G
NM_006477.4:c.*362A>G	NP_006468.1:n.*362A>G
XM_011529821.1:c.*362A>G	XP_011528123.1:n.*362A>G
XM_011529822.1:c.*362A>G	XP_011528124.1:n.*362A>G
XM_011529823.1:c.*362A>G	XP_011528125.1:n.*362A>G
NM_006477.5:c.*362A>G MANE Select	NP_006468.1:n.*362A>G