Canonical Allele Identifier: CA2400518775

Gene: RASL10A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313180A= , CM000684.2:g.29313180A=	GRCh38
NC_000022.10:g.29709169A= , CM000684.1:g.29709169A=	GRCh37
NC_000022.9:g.28039169A=	NCBI36
NG_032959.1:g.11174A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216101.7:c.*121T= MANE Select	ENSP00000216101.6:n.*121T=
ENST00000216101.6:c.*121T=	ENSP00000216101.6:n.*121T=
ENST00000401450.3:c.*679T=	ENSP00000386095.3:n.*679T=
NM_006477.4:c.*121T=	NP_006468.1:n.*121T=
XM_011529821.1:c.*121T=	XP_011528123.1:n.*121T=
XM_011529822.1:c.*121T=	XP_011528124.1:n.*121T=
XM_011529823.1:c.*121T=	XP_011528125.1:n.*121T=
NM_006477.5:c.*121T= MANE Select	NP_006468.1:n.*121T=