Canonical Allele Identifier: CA35919037

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198754608G>A , CM000663.2:g.198754608G>A	GRCh38
NC_000001.10:g.198723737G>A , CM000663.1:g.198723737G>A	GRCh37
NC_000001.9:g.196990360G>A	NCBI36
NG_007730.1:g.120513G>A
NG_007730.2:g.120514G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002838.5:c.3645+204G>A MANE Select	NP_002829.3:n.3645+204G>A
ENST00000442510.8:c.3645+204G>A MANE Select	ENSP00000411355.3:n.3645+204G>A
NM_002838.4:c.3645+204G>A	NP_002829.3:n.3645+204G>A
NM_080921.3:c.3162+204G>A	NP_563578.2:n.3162+204G>A
NM_080921.4:c.3162+204G>A	NP_563578.2:n.3162+204G>A
ENST00000348564.10:c.3162+204G>A	ENSP00000306782.7:n.3162+204G>A
ENST00000348564.11:c.3162+204G>A	ENSP00000306782.7:n.3162+204G>A
ENST00000442510.6:c.3645+204G>A	ENSP00000411355.3:n.3645+204G>A
ENST00000491302.2:n.2698+204G>A
ENST00000697631.1:c.3360+204G>A	ENSP00000513363.1:n.3360+204G>A
ENST00000697632.1:c.2607+204G>A	ENSP00000513364.1:n.2607+204G>A
ENST00000697633.1:c.2252+204G>A
ENST00000697635.1:n.598+204G>A
XM_006711472.2:c.3501+204G>A	XP_006711535.1:n.3501+204G>A
XM_006711472.4:c.3501+204G>A	XP_006711535.1:n.3501+204G>A
XM_006711473.2:c.3447+204G>A	XP_006711536.1:n.3447+204G>A
XM_006711473.3:c.3447+204G>A	XP_006711536.1:n.3447+204G>A
XM_006711474.2:c.3303+204G>A	XP_006711537.1:n.3303+204G>A
XM_006711474.3:c.3303+204G>A	XP_006711537.1:n.3303+204G>A