Canonical Allele Identifier: CA1024911975

Gene: RASL10A

Linked Data

• dbSNP Id: rs2061428779
• gnomAD v3: 22-29313165-G-A
• gnomAD v4: 22-29313165-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313165G>A , CM000684.2:g.29313165G>A	GRCh38
NC_000022.10:g.29709154G>A , CM000684.1:g.29709154G>A	GRCh37
NC_000022.9:g.28039154G>A	NCBI36
NG_032959.1:g.11159G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216101.7:c.*136C>T MANE Select	ENSP00000216101.6:n.*136C>T
ENST00000216101.6:c.*136C>T	ENSP00000216101.6:n.*136C>T
ENST00000401450.3:c.*694C>T	ENSP00000386095.3:n.*694C>T
NM_006477.4:c.*136C>T	NP_006468.1:n.*136C>T
XM_011529821.1:c.*136C>T	XP_011528123.1:n.*136C>T
XM_011529822.1:c.*136C>T	XP_011528124.1:n.*136C>T
XM_011529823.1:c.*136C>T	XP_011528125.1:n.*136C>T
NM_006477.5:c.*136C>T MANE Select	NP_006468.1:n.*136C>T