Canonical Allele Identifier: CA2400518787

Gene: RASL10A

Linked Data

• dbSNP Id: rs2061429085

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313205G>C , CM000684.2:g.29313205G>C	GRCh38
NC_000022.10:g.29709194G>C , CM000684.1:g.29709194G>C	GRCh37
NC_000022.9:g.28039194G>C	NCBI36
NG_032959.1:g.11199G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216101.7:c.*96C>G MANE Select	ENSP00000216101.6:n.*96C>G
ENST00000216101.6:c.*96C>G	ENSP00000216101.6:n.*96C>G
ENST00000401450.3:c.*654C>G	ENSP00000386095.3:n.*654C>G
NM_006477.4:c.*96C>G	NP_006468.1:n.*96C>G
XM_011529821.1:c.*96C>G	XP_011528123.1:n.*96C>G
XM_011529822.1:c.*96C>G	XP_011528124.1:n.*96C>G
XM_011529823.1:c.*96C>G	XP_011528125.1:n.*96C>G
NM_006477.5:c.*96C>G MANE Select	NP_006468.1:n.*96C>G