Canonical Allele Identifier: CA1139840877

Gene: SH2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156815190T= , CM000663.2:g.156815190T=	GRCh38
NC_000001.10:g.156784982T= , CM000663.1:g.156784982T=	GRCh37
NC_000001.9:g.155051606T=	NCBI36
NG_007493.1:g.4441T= , LRG_261:g.4441T=
NG_016849.1:g.6659A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368199.8:c.155A= MANE Select	ENSP00000357182.3:p.Asn52=
ENST00000368198.7:c.101A=	ENSP00000357181.3:p.Asn34=
ENST00000368199.7:c.155A=	ENSP00000357182.3:p.Asn52=
ENST00000392306.2:c.155A=	ENSP00000376123.2:p.Asn52=
ENST00000486350.1:n.222A=
ENST00000495306.1:n.207A=
NM_001161441.1:c.155A=	NP_001154913.1:p.Asn52=
NM_001161442.1:c.101A=	NP_001154914.1:p.Asn34=
NM_001161443.1:c.71A=	NP_001154915.1:p.Asn24=
NM_001161444.1:c.155A=	NP_001154916.1:p.Asn52=
NM_003975.3:c.155A=	NP_003966.2:p.Asn52=
XM_006711615.1:c.173A=	XP_006711678.1:p.Asn58=
XM_011510113.1:c.161A=	XP_011508415.1:p.Asn54=
XM_011510114.1:c.89A=	XP_011508416.1:p.Asn30=
XM_011510115.1:c.173A=	XP_011508417.1:p.Asn58=
XM_006711615.2:c.173A=	XP_006711678.1:p.Asn58=
XM_017002762.2:c.173A=	XP_016858251.1:p.Asn58=
XM_017002763.1:c.161A=	XP_016858252.1:p.Asn54=
XM_017002764.2:c.143A=	XP_016858253.1:p.Asn48=
XM_017002765.1:c.101A=	XP_016858254.1:p.Asn34=
XM_017002766.1:c.89A=	XP_016858255.1:p.Asn30=
XM_017002767.1:c.173A=	XP_016858256.1:p.Asn58=
NM_001161442.2:c.101A=	NP_001154914.1:p.Asn34=
NM_001161443.2:c.71A=	NP_001154915.1:p.Asn24=
NM_001161444.2:c.155A=	NP_001154916.1:p.Asn52=
NM_003975.4:c.155A= MANE Select	NP_003966.2:p.Asn52=
NM_001161441.2:c.155A=	NP_001154913.1:p.Asn52=