Canonical Allele Identifier: CA36183065

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198704256A>G , CM000663.2:g.198704256A>G	GRCh38
NC_000001.10:g.198673385A>G , CM000663.1:g.198673385A>G	GRCh37
NC_000001.9:g.196940008A>G	NCBI36
NG_007730.1:g.70161A>G
NG_007730.2:g.70162A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002838.5:c.659-216A>G MANE Select	NP_002829.3:n.659-216A>G
ENST00000442510.8:c.659-216A>G MANE Select	ENSP00000411355.3:n.659-216A>G
NM_002838.4:c.659-216A>G	NP_002829.3:n.659-216A>G
NM_080921.3:c.176-216A>G	NP_563578.2:n.176-216A>G
NM_080921.4:c.176-216A>G	NP_563578.2:n.176-216A>G
ENST00000348564.10:c.176-216A>G	ENSP00000306782.7:n.176-216A>G
ENST00000348564.11:c.176-216A>G	ENSP00000306782.7:n.176-216A>G
ENST00000367367.8:c.461-216A>G	ENSP00000356337.5:n.461-216A>G
ENST00000367379.5:c.176-216A>G	ENSP00000356349.2:n.176-216A>G
ENST00000367379.6:c.176-216A>G	ENSP00000356349.2:n.176-216A>G
ENST00000442510.6:c.659-216A>G	ENSP00000411355.3:n.659-216A>G
ENST00000529828.5:c.515-216A>G	ENSP00000469141.1:n.515-216A>G
ENST00000530727.5:c.317-216A>G	ENSP00000433536.2:n.317-216A>G
ENST00000643513.1:c.317-216A>G	ENSP00000494132.1:n.317-216A>G
ENST00000645247.1:c.440-216A>G	ENSP00000494327.1:n.440-216A>G
ENST00000697630.1:n.1145A>G
ENST00000697631.1:c.374-216A>G	ENSP00000513363.1:n.374-216A>G
ENST00000697632.1:c.-380-216A>G	ENSP00000513364.1:n.-380-216A>G
XM_006711472.2:c.515-216A>G	XP_006711535.1:n.515-216A>G
XM_006711472.4:c.515-216A>G	XP_006711535.1:n.515-216A>G
XM_006711473.2:c.461-216A>G	XP_006711536.1:n.461-216A>G
XM_006711473.3:c.461-216A>G	XP_006711536.1:n.461-216A>G
XM_006711474.2:c.317-216A>G	XP_006711537.1:n.317-216A>G
XM_006711474.3:c.317-216A>G	XP_006711537.1:n.317-216A>G