Canonical Allele Identifier: CA1314697

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198709705A>G , CM000663.2:g.198709705A>G	GRCh38
NC_000001.10:g.198678834A>G , CM000663.1:g.198678834A>G	GRCh37
NC_000001.9:g.196945457A>G	NCBI36
NG_007730.1:g.75610A>G
NG_007730.2:g.75611A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697630.1:n.1754A>G
ENST00000697631.1:c.767A>G	ENSP00000513363.1:p.Asn256Ser
ENST00000697632.1:c.14A>G	ENSP00000513364.1:p.Asn5Ser
ENST00000348564.11:c.569A>G	ENSP00000306782.7:p.Asn190Ser
ENST00000442510.8:c.1052A>G MANE Select	ENSP00000411355.3:p.Asn351Ser
ENST00000348564.10:c.569A>G	ENSP00000306782.7:p.Asn190Ser
ENST00000367367.8:c.854A>G	ENSP00000356337.5:p.Asn285Ser
ENST00000442510.6:c.1052A>G	ENSP00000411355.3:p.Asn351Ser
ENST00000529828.5:c.908A>G	ENSP00000469141.1:p.Asn303Ser
ENST00000530727.5:c.710A>G	ENSP00000433536.2:p.Asn237Ser
NM_002838.4:c.1052A>G	NP_002829.3:p.Asn351Ser
NM_080921.3:c.569A>G	NP_563578.2:p.Asn190Ser
XM_006711472.2:c.908A>G	XP_006711535.1:p.Asn303Ser
XM_006711473.2:c.854A>G	XP_006711536.1:p.Asn285Ser
XM_006711474.2:c.710A>G	XP_006711537.1:p.Asn237Ser
XM_006711472.4:c.908A>G	XP_006711535.1:p.Asn303Ser
XM_006711473.3:c.854A>G	XP_006711536.1:p.Asn285Ser
XM_006711474.3:c.710A>G	XP_006711537.1:p.Asn237Ser
NM_002838.5:c.1052A>G MANE Select	NP_002829.3:p.Asn351Ser
NM_080921.4:c.569A>G	NP_563578.2:p.Asn190Ser