Canonical Allele Identifier: CA3191757879
Community Standard Title: NM_001005242.3(PKP2):c.1211T= (p.Leu404=)
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32850933A= , CM000674.2:g.32850933A= GRCh38
NC_000012.11:g.33003867A= , CM000674.1:g.33003867A= GRCh37
NC_000012.10:g.32895134A= NCBI36
NG_009000.1:g.50914T= , LRG_398:g.50914T=

Transcript Alleles

HGVS Amino-acid Change
NM_001005242.3:c.1211T= MANE Select NP_001005242.2:p.Leu404=
ENST00000340811.9:c.1211T= MANE Select ENSP00000342800.5:p.Leu404=
NM_001005242.2:c.1211T= NP_001005242.2:p.Leu404=
NM_004572.3:c.1211T= , LRG_398t1:c.1211T= NP_004563.2:p.Leu404=
NM_004572.4:c.1211T= NP_004563.2:p.Leu404=
ENST00000070846.10:c.1211T= ENSP00000070846.6:p.Leu404=
ENST00000070846.11:c.1211T= ENSP00000070846.6:p.Leu404=
ENST00000340811.8:c.1211T= ENSP00000342800.4:p.Leu404=
ENST00000613243.1:c.1211T= ENSP00000478295.1:p.Leu404=
ENST00000700559.1:c.426T=
ENST00000700559.2:c.1211T= ENSP00000515065.2:p.Leu404=
ENST00000700560.1:n.426T=
ENST00000700561.1:n.552T=
ENST00000700563.1:c.1165T=
ENST00000700563.2:c.1211T= ENSP00000515066.2:p.Leu404=
ENST00000700564.1:n.1215T=
ENST00000700565.1:n.1064T=