Canonical Allele Identifier: CA1829832695

Gene: PLGRKT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5372489G= , CM000671.2:g.5372489G=	GRCh38
NC_000009.11:g.5372489G= , CM000671.1:g.5372489G=	GRCh37
NC_000009.10:g.5362489G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223864.7:c.82-10601C= MANE Select	ENSP00000223864.2:n.82-10601C=
ENST00000223864.6:c.82-10601C=	ENSP00000223864.2:n.82-10601C=
ENST00000472145.5:n.289-10601C=
ENST00000482696.5:n.461+9374C=
NM_018465.3:c.82-10601C=	NP_060935.2:n.82-10601C=
XM_005251510.3:c.82-10601C=	XP_005251567.1:n.82-10601C=
XM_005251512.3:c.-19+9374C=	XP_005251569.1:n.-19+9374C=
XM_011517960.1:c.82-10601C=	XP_011516262.1:n.82-10601C=
XM_005251510.5:c.82-10601C=	XP_005251567.1:n.82-10601C=
XM_005251512.4:c.-19+9374C=	XP_005251569.1:n.-19+9374C=
XM_011517960.2:c.82-10601C=	XP_011516262.1:n.82-10601C=
NM_018465.4:c.82-10601C= MANE Select	NP_060935.2:n.82-10601C=