Canonical Allele Identifier: CA865148441

Gene: PLGRKT

Linked Data

• dbSNP Id: rs1415561720
• gnomAD v3: 9-5372337-G-A
• gnomAD v4: 9-5372337-G-A
• MyVariant Identifiers: chr9:g.5372337G>A (hg19) ; chr9:g.5372337G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5372337G>A , CM000671.2:g.5372337G>A	GRCh38
NC_000009.11:g.5372337G>A , CM000671.1:g.5372337G>A	GRCh37
NC_000009.10:g.5362337G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000223864.7:c.82-10449C>T MANE Select	ENSP00000223864.2:n.82-10449C>T
ENST00000223864.6:c.82-10449C>T	ENSP00000223864.2:n.82-10449C>T
ENST00000472145.5:n.289-10449C>T
ENST00000482696.5:n.461+9526C>T
NM_018465.3:c.82-10449C>T	NP_060935.2:n.82-10449C>T
XM_005251510.3:c.82-10449C>T	XP_005251567.1:n.82-10449C>T
XM_005251512.3:c.-19+9526C>T	XP_005251569.1:n.-19+9526C>T
XM_011517960.1:c.82-10449C>T	XP_011516262.1:n.82-10449C>T
XM_005251510.5:c.82-10449C>T	XP_005251567.1:n.82-10449C>T
XM_005251512.4:c.-19+9526C>T	XP_005251569.1:n.-19+9526C>T
XM_011517960.2:c.82-10449C>T	XP_011516262.1:n.82-10449C>T
NM_018465.4:c.82-10449C>T MANE Select	NP_060935.2:n.82-10449C>T