Canonical Allele Identifier: CA342932726

Gene: SH2D2A

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368199.8:c.155A>C MANE Select	ENSP00000357182.3:p.Asn52Thr
ENST00000368198.7:c.101A>C	ENSP00000357181.3:p.Asn34Thr
ENST00000368199.7:c.155A>C	ENSP00000357182.3:p.Asn52Thr
ENST00000392306.2:c.155A>C	ENSP00000376123.2:p.Asn52Thr
ENST00000486350.1:n.222A>C
ENST00000495306.1:n.207A>C
NM_001161441.1:c.155A>C	NP_001154913.1:p.Asn52Thr
NM_001161442.1:c.101A>C	NP_001154914.1:p.Asn34Thr
NM_001161443.1:c.71A>C	NP_001154915.1:p.Asn24Thr
NM_001161444.1:c.155A>C	NP_001154916.1:p.Asn52Thr
NM_003975.3:c.155A>C	NP_003966.2:p.Asn52Thr
XM_006711615.1:c.173A>C	XP_006711678.1:p.Asn58Thr
XM_011510113.1:c.161A>C	XP_011508415.1:p.Asn54Thr
XM_011510114.1:c.89A>C	XP_011508416.1:p.Asn30Thr
XM_011510115.1:c.173A>C	XP_011508417.1:p.Asn58Thr
XM_006711615.2:c.173A>C	XP_006711678.1:p.Asn58Thr
XM_017002762.2:c.173A>C	XP_016858251.1:p.Asn58Thr
XM_017002763.1:c.161A>C	XP_016858252.1:p.Asn54Thr
XM_017002764.2:c.143A>C	XP_016858253.1:p.Asn48Thr
XM_017002765.1:c.101A>C	XP_016858254.1:p.Asn34Thr
XM_017002766.1:c.89A>C	XP_016858255.1:p.Asn30Thr
XM_017002767.1:c.173A>C	XP_016858256.1:p.Asn58Thr
NM_001161442.2:c.101A>C	NP_001154914.1:p.Asn34Thr
NM_001161443.2:c.71A>C	NP_001154915.1:p.Asn24Thr
NM_001161444.2:c.155A>C	NP_001154916.1:p.Asn52Thr
NM_003975.4:c.155A>C MANE Select	NP_003966.2:p.Asn52Thr
NM_001161441.2:c.155A>C	NP_001154913.1:p.Asn52Thr