Canonical Allele Identifier: CA1829832622
Gene: PLGRKT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5372345C= , CM000671.2:g.5372345C= GRCh38
NC_000009.11:g.5372345C= , CM000671.1:g.5372345C= GRCh37
NC_000009.10:g.5362345C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000223864.7:c.82-10457G= MANE Select ENSP00000223864.2:n.82-10457G=
ENST00000223864.6:c.82-10457G= ENSP00000223864.2:n.82-10457G=
ENST00000472145.5:n.289-10457G=
ENST00000482696.5:n.461+9518G=
NM_018465.3:c.82-10457G= NP_060935.2:n.82-10457G=
XM_005251510.3:c.82-10457G= XP_005251567.1:n.82-10457G=
XM_005251512.3:c.-19+9518G= XP_005251569.1:n.-19+9518G=
XM_011517960.1:c.82-10457G= XP_011516262.1:n.82-10457G=
XM_005251510.5:c.82-10457G= XP_005251567.1:n.82-10457G=
XM_005251512.4:c.-19+9518G= XP_005251569.1:n.-19+9518G=
XM_011517960.2:c.82-10457G= XP_011516262.1:n.82-10457G=
NM_018465.4:c.82-10457G= MANE Select NP_060935.2:n.82-10457G=