Canonical Allele Identifier: CA2026396981

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822526G= , CM000674.2:g.32822526G=	GRCh38
NC_000012.11:g.32975460G= , CM000674.1:g.32975460G=	GRCh37
NC_000012.10:g.32866727G=	NCBI36
NG_009000.1:g.79321C= , LRG_398:g.79321C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001005242.3:c.1780C= MANE Select	NP_001005242.2:p.Gln594=
ENST00000340811.9:c.1780C= MANE Select	ENSP00000342800.5:p.Gln594=
NM_001005242.2:c.1780C=	NP_001005242.2:p.Gln594=
NM_004572.3:c.1912C= , LRG_398t1:c.1912C=	NP_004563.2:p.Gln638=
NM_004572.4:c.1912C=	NP_004563.2:p.Gln638=
ENST00000070846.10:c.1912C=	ENSP00000070846.6:p.Gln638=
ENST00000070846.11:c.1912C=	ENSP00000070846.6:p.Gln638=
ENST00000340811.8:c.1780C=	ENSP00000342800.4:p.Gln594=
ENST00000546498.1:n.467C=
ENST00000546498.2:n.467C=
ENST00000552612.5:n.201C=
ENST00000613243.1:c.1912C=	ENSP00000478295.1:p.Gln638=
ENST00000700555.1:c.220C=	ENSP00000515062.1:p.Gln74=
ENST00000700555.2:n.292C=
ENST00000700556.1:c.251C=
ENST00000700559.1:c.995C=
ENST00000700559.2:c.1780C=	ENSP00000515065.2:p.Gln594=
ENST00000700560.1:n.995C=
ENST00000700561.1:n.1121C=
ENST00000700563.1:c.1734C=
ENST00000700563.2:c.1780C=	ENSP00000515066.2:p.Gln594=
ENST00000700564.1:n.1784C=