Canonical Allele Identifier: CA384364643

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32977011C>A (hg19) ; chr12:g.32824077C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32824077C>A , CM000674.2:g.32824077C>A	GRCh38
NC_000012.11:g.32977011C>A , CM000674.1:g.32977011C>A	GRCh37
NC_000012.10:g.32868278C>A	NCBI36
NG_009000.1:g.77770G>T , LRG_398:g.77770G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.154G>T
ENST00000700559.2:c.1642G>T	ENSP00000515065.2:p.Gly548Ter
ENST00000700563.2:c.1642G>T	ENSP00000515066.2:p.Gly548Ter
ENST00000546498.2:n.329G>T
ENST00000700555.1:c.82G>T	ENSP00000515062.1:p.Gly28Ter
ENST00000700556.1:c.113G>T
ENST00000700559.1:c.857G>T
ENST00000700560.1:n.857G>T
ENST00000700561.1:n.983G>T
ENST00000700563.1:c.1596G>T
ENST00000700564.1:n.1646G>T
ENST00000070846.11:c.1774G>T	ENSP00000070846.6:p.Gly592Ter
ENST00000340811.9:c.1642G>T MANE Select	ENSP00000342800.5:p.Gly548Ter
ENST00000070846.10:c.1774G>T	ENSP00000070846.6:p.Gly592Ter
ENST00000340811.8:c.1642G>T	ENSP00000342800.4:p.Gly548Ter
ENST00000546498.1:n.329G>T
ENST00000552612.5:n.63G>T
ENST00000613243.1:c.1774G>T	ENSP00000478295.1:p.Gly592Ter
NM_001005242.2:c.1642G>T	NP_001005242.2:p.Gly548Ter
NM_004572.3:c.1774G>T , LRG_398t1:c.1774G>T	NP_004563.2:p.Gly592Ter
NM_001005242.3:c.1642G>T MANE Select	NP_001005242.2:p.Gly548Ter
NM_004572.4:c.1774G>T	NP_004563.2:p.Gly592Ter