Canonical Allele Identifier: CA16042610
Gene: RASA1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 373353
ClinVar RCV Id: RCV000414450
dbSNP Id: rs1057518367

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268995G>A , CM000667.2:g.87268995G>A GRCh38
NC_000005.9:g.86564812G>A , CM000667.1:g.86564812G>A GRCh37
NC_000005.8:g.86600568G>A NCBI36
NG_011650.1:g.5662G>A

Transcript Alleles

HGVS Amino-acid change
NM_002890.2:c.539+5G>A VV NP_002881.1:p.=
NM_022650.2:c.-53G>A VV NP_072179.1:p.=
XM_011543525.1:c.539+5G>A XP_011541827.1:p.=
XM_011543526.1:c.539+5G>A XP_011541828.1:p.=
XM_011543527.1:c.539+5G>A XP_011541829.1:p.=
XM_011543525.2:c.539+5G>A
XM_011543527.3:c.539+5G>A
ENST00000274376.10:c.539+5G>A ENSP00000274376.6:p.=
ENST00000456692.6:c.-53G>A ENSP00000411221.2:p.=
ENST00000506290.1:c.-66G>A ENSP00000420905.1:p.=
ENST00000512763.5:c.-150G>A ENSP00000422008.1:p.=
ENST00000515800.6:c.539+5G>A ENSP00000423395.2:p.=