Canonical Allele Identifier: CA2645158

Gene: RASA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141516426G>A , CM000665.2:g.141516426G>A	GRCh38
NC_000003.11:g.141235268G>A , CM000665.1:g.141235268G>A	GRCh37
NC_000003.10:g.142717958G>A	NCBI36
NG_042187.1:g.34380G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286364.9:c.350G>A MANE Select	ENSP00000286364.3:p.Arg117His
ENST00000286364.7:c.350G>A	ENSP00000286364.3:p.Arg117His
ENST00000452898.2:c.350G>A	ENSP00000391677.2:p.Arg117His
ENST00000515549.1:c.*172G>A	ENSP00000424293.1:n.*172G>A
NM_001303245.1:c.350G>A	NP_001290174.1:p.Arg117His
NM_001303246.1:c.350G>A	NP_001290175.1:p.Arg117His
NM_006506.3:c.350G>A	NP_006497.2:p.Arg117His
XM_011513059.1:c.359G>A	XP_011511361.1:p.Arg120His
XM_011513059.2:c.359G>A	XP_011511361.1:p.Arg120His
XM_017006968.1:c.416G>A	XP_016862457.1:p.Arg139His
XM_017006969.1:c.416G>A	XP_016862458.1:p.Arg139His
XM_017006970.1:c.416G>A	XP_016862459.1:p.Arg139His
XM_017006971.1:c.416G>A	XP_016862460.1:p.Arg139His
XM_024453691.1:c.176G>A	XP_024309459.1:p.Arg59His
NM_001303245.2:c.350G>A	NP_001290174.1:p.Arg117His
NM_001303246.2:c.350G>A	NP_001290175.1:p.Arg117His
NM_006506.5:c.350G>A MANE Select	NP_006497.2:p.Arg117His
NM_001303245.3:c.350G>A	NP_001290174.1:p.Arg117His
NM_001303246.3:c.350G>A	NP_001290175.1:p.Arg117His