Canonical Allele Identifier: CA865148456

Gene: PLGRKT

Linked Data

• dbSNP Id: rs1274877064
• MyVariant Identifiers: chr9:g.5372359C>G (hg19) ; chr9:g.5372359C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5372359C>G , CM000671.2:g.5372359C>G	GRCh38
NC_000009.11:g.5372359C>G , CM000671.1:g.5372359C>G	GRCh37
NC_000009.10:g.5362359C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223864.7:c.82-10471G>C MANE Select	ENSP00000223864.2:n.82-10471G>C
ENST00000223864.6:c.82-10471G>C	ENSP00000223864.2:n.82-10471G>C
ENST00000472145.5:n.289-10471G>C
ENST00000482696.5:n.461+9504G>C
NM_018465.3:c.82-10471G>C	NP_060935.2:n.82-10471G>C
XM_005251510.3:c.82-10471G>C	XP_005251567.1:n.82-10471G>C
XM_005251512.3:c.-19+9504G>C	XP_005251569.1:n.-19+9504G>C
XM_011517960.1:c.82-10471G>C	XP_011516262.1:n.82-10471G>C
XM_005251510.5:c.82-10471G>C	XP_005251567.1:n.82-10471G>C
XM_005251512.4:c.-19+9504G>C	XP_005251569.1:n.-19+9504G>C
XM_011517960.2:c.82-10471G>C	XP_011516262.1:n.82-10471G>C
NM_018465.4:c.82-10471G>C MANE Select	NP_060935.2:n.82-10471G>C