Canonical Allele Identifier: CA1829832599

Gene: PLGRKT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5372302_5372305delinsAAAT , CM000671.2:g.5372302_5372305delinsAAAT	GRCh38
NC_000009.11:g.5372302_5372305delinsAAAT , CM000671.1:g.5372302_5372305delinsAAAT	GRCh37
NC_000009.10:g.5362302_5362305delinsAAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223864.7:c.82-10417_82-10414delinsATTT MANE Select	ENSP00000223864.2:n.82-10417_82-10414delinsATTT
ENST00000223864.6:c.82-10417_82-10414delinsATTT	ENSP00000223864.2:n.82-10417_82-10414delinsATTT
ENST00000472145.5:n.289-10417_289-10414delinsATTT
ENST00000482696.5:n.461+9558_461+9561delinsATTT
NM_018465.3:c.82-10417_82-10414delinsATTT	NP_060935.2:n.82-10417_82-10414delinsATTT
XM_005251510.3:c.82-10417_82-10414delinsATTT	XP_005251567.1:n.82-10417_82-10414delinsATTT
XM_005251512.3:c.-19+9558_-19+9561delinsATTT	XP_005251569.1:n.-19+9558_-19+9561delinsATTT
XM_011517960.1:c.82-10417_82-10414delinsATTT	XP_011516262.1:n.82-10417_82-10414delinsATTT
XM_005251510.5:c.82-10417_82-10414delinsATTT	XP_005251567.1:n.82-10417_82-10414delinsATTT
XM_005251512.4:c.-19+9558_-19+9561delinsATTT	XP_005251569.1:n.-19+9558_-19+9561delinsATTT
XM_011517960.2:c.82-10417_82-10414delinsATTT	XP_011516262.1:n.82-10417_82-10414delinsATTT
NM_018465.4:c.82-10417_82-10414delinsATTT MANE Select	NP_060935.2:n.82-10417_82-10414delinsATTT