Canonical Allele Identifier: CA292984

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198708257G>A , CM000663.2:g.198708257G>A	GRCh38
NC_000001.10:g.198677386G>A , CM000663.1:g.198677386G>A	GRCh37
NC_000001.9:g.196944009G>A	NCBI36
NG_007730.1:g.74162G>A
NG_007730.2:g.74163G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697630.1:n.1731G>A
ENST00000697631.1:c.744G>A	ENSP00000513363.1:p.Gln248=
ENST00000697632.1:c.-10G>A	ENSP00000513364.1:n.-10G>A
ENST00000348564.11:c.546G>A	ENSP00000306782.7:p.Gln182=
ENST00000442510.8:c.1029G>A MANE Select	ENSP00000411355.3:p.Gln343=
ENST00000348564.10:c.546G>A	ENSP00000306782.7:p.Gln182=
ENST00000367367.8:c.831G>A	ENSP00000356337.5:p.Gln277=
ENST00000442510.6:c.1029G>A	ENSP00000411355.3:p.Gln343=
ENST00000529828.5:c.885G>A	ENSP00000469141.1:p.Gln295=
ENST00000530727.5:c.687G>A	ENSP00000433536.2:p.Gln229=
NM_002838.4:c.1029G>A	NP_002829.3:p.Gln343=
NM_080921.3:c.546G>A	NP_563578.2:p.Gln182=
XM_006711472.2:c.885G>A	XP_006711535.1:p.Gln295=
XM_006711473.2:c.831G>A	XP_006711536.1:p.Gln277=
XM_006711474.2:c.687G>A	XP_006711537.1:p.Gln229=
XM_006711472.4:c.885G>A	XP_006711535.1:p.Gln295=
XM_006711473.3:c.831G>A	XP_006711536.1:p.Gln277=
XM_006711474.3:c.687G>A	XP_006711537.1:p.Gln229=
NM_002838.5:c.1029G>A MANE Select	NP_002829.3:p.Gln343=
NM_080921.4:c.546G>A	NP_563578.2:p.Gln182=