Canonical Allele Identifier: CA653145305

Gene: PLGRKT

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5372266_5372267insC , CM000671.2:g.5372266_5372267insC	GRCh38
NC_000009.11:g.5372266_5372267insC , CM000671.1:g.5372266_5372267insC	GRCh37
NC_000009.10:g.5362266_5362267insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223864.7:c.82-10379_82-10378insG MANE Select	ENSP00000223864.2:n.82-10379_82-10378insG
ENST00000223864.6:c.82-10379_82-10378insG	ENSP00000223864.2:n.82-10379_82-10378insG
ENST00000472145.5:n.289-10379_289-10378insG
ENST00000482696.5:n.461+9596_461+9597insG
NM_018465.3:c.82-10379_82-10378insG	NP_060935.2:n.82-10379_82-10378insG
XM_005251510.3:c.82-10379_82-10378insG	XP_005251567.1:n.82-10379_82-10378insG
XM_005251512.3:c.-19+9596_-19+9597insG	XP_005251569.1:n.-19+9596_-19+9597insG
XM_011517960.1:c.82-10379_82-10378insG	XP_011516262.1:n.82-10379_82-10378insG
XM_005251510.5:c.82-10379_82-10378insG	XP_005251567.1:n.82-10379_82-10378insG
XM_005251512.4:c.-19+9596_-19+9597insG	XP_005251569.1:n.-19+9596_-19+9597insG
XM_011517960.2:c.82-10379_82-10378insG	XP_011516262.1:n.82-10379_82-10378insG
NM_018465.4:c.82-10379_82-10378insG MANE Select	NP_060935.2:n.82-10379_82-10378insG