Canonical Allele Identifier: CA2645416

Gene: RASA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141571464C>G , CM000665.2:g.141571464C>G	GRCh38
NC_000003.11:g.141290306C>G , CM000665.1:g.141290306C>G	GRCh37
NC_000003.10:g.142772996C>G	NCBI36
NG_042187.1:g.89418C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286364.9:c.1079C>G MANE Select	ENSP00000286364.3:p.Ala360Gly
ENST00000286364.7:c.1079C>G	ENSP00000286364.3:p.Ala360Gly
ENST00000452898.2:c.1079C>G	ENSP00000391677.2:p.Ala360Gly
NM_001303245.1:c.1079C>G	NP_001290174.1:p.Ala360Gly
NM_001303246.1:c.1079C>G	NP_001290175.1:p.Ala360Gly
NM_006506.3:c.1079C>G	NP_006497.2:p.Ala360Gly
XM_011513059.1:c.1088C>G	XP_011511361.1:p.Ala363Gly
XM_011513060.1:c.416C>G	XP_011511362.1:p.Ala139Gly
XM_011513059.2:c.1088C>G	XP_011511361.1:p.Ala363Gly
XM_017006968.1:c.1145C>G	XP_016862457.1:p.Ala382Gly
XM_017006969.1:c.1145C>G	XP_016862458.1:p.Ala382Gly
XM_017006970.1:c.1145C>G	XP_016862459.1:p.Ala382Gly
XM_017006971.1:c.1145C>G	XP_016862460.1:p.Ala382Gly
XM_024453691.1:c.905C>G	XP_024309459.1:p.Ala302Gly
NM_001303245.2:c.1079C>G	NP_001290174.1:p.Ala360Gly
NM_001303246.2:c.1079C>G	NP_001290175.1:p.Ala360Gly
NM_006506.5:c.1079C>G MANE Select	NP_006497.2:p.Ala360Gly
NM_001303245.3:c.1079C>G	NP_001290174.1:p.Ala360Gly
NM_001303246.3:c.1079C>G	NP_001290175.1:p.Ala360Gly