Canonical Allele Identifier: CA865148402

Gene: PLGRKT

Linked Data

• dbSNP Id: rs1369953441
• gnomAD v3: 9-5372238-C-CA
• gnomAD v4: 9-5372238-C-CA
• MyVariant Identifiers: chr9:g.5372238_5372239insA (hg19) ; chr9:g.5372238_5372239insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5372241dup , CM000671.2:g.5372241dup	GRCh38
NC_000009.11:g.5372241dup , CM000671.1:g.5372241dup	GRCh37
NC_000009.10:g.5362241dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223864.7:c.82-10351dup MANE Select	ENSP00000223864.2:n.82-10351dup
ENST00000223864.6:c.82-10351dup	ENSP00000223864.2:n.82-10351dup
ENST00000472145.5:n.289-10351dup
ENST00000482696.5:n.461+9624dup
NM_018465.3:c.82-10351dup	NP_060935.2:n.82-10351dup
XM_005251510.3:c.82-10351dup	XP_005251567.1:n.82-10351dup
XM_005251512.3:c.-19+9624dup	XP_005251569.1:n.-19+9624dup
XM_011517960.1:c.82-10351dup	XP_011516262.1:n.82-10351dup
XM_005251510.5:c.82-10351dup	XP_005251567.1:n.82-10351dup
XM_005251512.4:c.-19+9624dup	XP_005251569.1:n.-19+9624dup
XM_011517960.2:c.82-10351dup	XP_011516262.1:n.82-10351dup
NM_018465.4:c.82-10351dup MANE Select	NP_060935.2:n.82-10351dup