Canonical Allele Identifier: CA2153613719

Gene: PTPN21

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88480278G= , CM000676.2:g.88480278G=	GRCh38
NC_000014.8:g.88946622G= , CM000676.1:g.88946622G=	GRCh37
NC_000014.7:g.88016375G=	NCBI36
NG_046949.1:g.79502C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556564.6:c.1153C= MANE Select	ENSP00000452414.1:p.Leu385=
ENST00000328736.7:c.1153C=	ENSP00000330276.3:p.Leu385=
ENST00000536337.5:c.*1090C=	ENSP00000443951.1:n.*1090C=
ENST00000554270.5:n.1266C=
ENST00000556564.5:c.1153C=	ENSP00000452414.1:p.Leu385=
NM_007039.3:c.1153C=	NP_008970.2:p.Leu385=
XM_005267287.1:c.1153C=	XP_005267344.1:p.Leu385=
XM_006720011.2:c.784C=	XP_006720074.1:p.Leu262=
XM_011536367.1:c.1153C=	XP_011534669.1:p.Leu385=
XM_011536368.1:c.784C=	XP_011534670.1:p.Leu262=
XM_011536369.1:c.541C=	XP_011534671.1:p.Leu181=
XM_005267287.3:c.1153C=	XP_005267344.1:p.Leu385=
XM_006720011.3:c.784C=	XP_006720074.1:p.Leu262=
XM_011536367.3:c.1153C=	XP_011534669.1:p.Leu385=
XM_011536368.2:c.784C=	XP_011534670.1:p.Leu262=
XM_011536369.2:c.541C=	XP_011534671.1:p.Leu181=
XM_017020938.2:c.784C=	XP_016876427.1:p.Leu262=
XM_017020939.1:c.541C=	XP_016876428.1:p.Leu181=
NM_007039.4:c.1153C= MANE Select	NP_008970.2:p.Leu385=