Canonical Allele Identifier: CA354782260

Gene: RASA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141586710T>C , CM000665.2:g.141586710T>C	GRCh38
NC_000003.11:g.141305552T>C , CM000665.1:g.141305552T>C	GRCh37
NC_000003.10:g.142788242T>C	NCBI36
NG_042187.1:g.104664T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286364.9:c.1891T>C MANE Select	ENSP00000286364.3:p.Phe631Leu
ENST00000286364.7:c.1891T>C	ENSP00000286364.3:p.Phe631Leu
ENST00000452898.2:c.1891T>C	ENSP00000391677.2:p.Phe631Leu
ENST00000506365.1:n.12T>C
ENST00000509032.5:n.385T>C
ENST00000509118.5:n.343T>C
NM_001303245.1:c.1891T>C	NP_001290174.1:p.Phe631Leu
NM_001303246.1:c.1891T>C	NP_001290175.1:p.Phe631Leu
NM_006506.3:c.1891T>C	NP_006497.2:p.Phe631Leu
XM_011513059.1:c.1900T>C	XP_011511361.1:p.Phe634Leu
XM_011513060.1:c.1228T>C	XP_011511362.1:p.Phe410Leu
XM_011513059.2:c.1900T>C	XP_011511361.1:p.Phe634Leu
XM_017006968.1:c.1957T>C	XP_016862457.1:p.Phe653Leu
XM_017006969.1:c.1957T>C	XP_016862458.1:p.Phe653Leu
XM_017006970.1:c.1957T>C	XP_016862459.1:p.Phe653Leu
XM_024453691.1:c.1717T>C	XP_024309459.1:p.Phe573Leu
NM_001303245.2:c.1891T>C	NP_001290174.1:p.Phe631Leu
NM_001303246.2:c.1891T>C	NP_001290175.1:p.Phe631Leu
NM_006506.5:c.1891T>C MANE Select	NP_006497.2:p.Phe631Leu
NM_001303245.3:c.1891T>C	NP_001290174.1:p.Phe631Leu
NM_001303246.3:c.1891T>C	NP_001290175.1:p.Phe631Leu