Canonical Allele Identifier: CA384364760
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32824094A>T , CM000674.2:g.32824094A>T GRCh38
NC_000012.11:g.32977028A>T , CM000674.1:g.32977028A>T GRCh37
NC_000012.10:g.32868295A>T NCBI36
NG_009000.1:g.77753T>A , LRG_398:g.77753T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.137T>A
ENST00000700559.2:c.1625T>A ENSP00000515065.2:p.Leu542Gln
ENST00000700563.2:c.1625T>A ENSP00000515066.2:p.Leu542Gln
ENST00000546498.2:n.312T>A
ENST00000700555.1:c.65T>A ENSP00000515062.1:p.Leu22Gln
ENST00000700556.1:c.96T>A
ENST00000700559.1:c.840T>A
ENST00000700560.1:n.840T>A
ENST00000700561.1:n.966T>A
ENST00000700563.1:c.1579T>A
ENST00000700564.1:n.1629T>A
ENST00000070846.11:c.1757T>A ENSP00000070846.6:p.Leu586Gln
ENST00000340811.9:c.1625T>A MANE Select ENSP00000342800.5:p.Leu542Gln
ENST00000070846.10:c.1757T>A ENSP00000070846.6:p.Leu586Gln
ENST00000340811.8:c.1625T>A ENSP00000342800.4:p.Leu542Gln
ENST00000546498.1:n.312T>A
ENST00000552612.5:n.46T>A
ENST00000613243.1:c.1757T>A ENSP00000478295.1:p.Leu586Gln
NM_001005242.2:c.1625T>A NP_001005242.2:p.Leu542Gln
NM_004572.3:c.1757T>A , LRG_398t1:c.1757T>A NP_004563.2:p.Leu586Gln
NM_001005242.3:c.1625T>A MANE Select NP_001005242.2:p.Leu542Gln
NM_004572.4:c.1757T>A NP_004563.2:p.Leu586Gln