Canonical Allele Identifier: CA35890000

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198709964G>A , CM000663.2:g.198709964G>A	GRCh38
NC_000001.10:g.198679093G>A , CM000663.1:g.198679093G>A	GRCh37
NC_000001.9:g.196945716G>A	NCBI36
NG_007730.1:g.75869G>A
NG_007730.2:g.75870G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002838.5:c.1171+140G>A MANE Select	NP_002829.3:n.1171+140G>A
ENST00000442510.8:c.1171+140G>A MANE Select	ENSP00000411355.3:n.1171+140G>A
NM_002838.4:c.1171+140G>A	NP_002829.3:n.1171+140G>A
NM_080921.3:c.688+140G>A	NP_563578.2:n.688+140G>A
NM_080921.4:c.688+140G>A	NP_563578.2:n.688+140G>A
ENST00000348564.10:c.688+140G>A	ENSP00000306782.7:n.688+140G>A
ENST00000348564.11:c.688+140G>A	ENSP00000306782.7:n.688+140G>A
ENST00000367367.8:c.973+140G>A	ENSP00000356337.5:n.973+140G>A
ENST00000442510.6:c.1171+140G>A	ENSP00000411355.3:n.1171+140G>A
ENST00000529828.5:c.1027+140G>A	ENSP00000469141.1:n.1027+140G>A
ENST00000530727.5:c.829+140G>A	ENSP00000433536.2:n.829+140G>A
ENST00000697630.1:n.2013G>A
ENST00000697631.1:c.886+140G>A	ENSP00000513363.1:n.886+140G>A
ENST00000697632.1:c.133+140G>A	ENSP00000513364.1:n.133+140G>A
XM_006711472.2:c.1027+140G>A	XP_006711535.1:n.1027+140G>A
XM_006711472.4:c.1027+140G>A	XP_006711535.1:n.1027+140G>A
XM_006711473.2:c.973+140G>A	XP_006711536.1:n.973+140G>A
XM_006711473.3:c.973+140G>A	XP_006711536.1:n.973+140G>A
XM_006711474.2:c.829+140G>A	XP_006711537.1:n.829+140G>A
XM_006711474.3:c.829+140G>A	XP_006711537.1:n.829+140G>A