Canonical Allele Identifier: CA384359723

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32955412C>A (hg19) ; chr12:g.32802478C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32802478C>A , CM000674.2:g.32802478C>A	GRCh38
NC_000012.11:g.32955412C>A , CM000674.1:g.32955412C>A	GRCh37
NC_000012.10:g.32846679C>A	NCBI36
NG_009000.1:g.99369G>T , LRG_398:g.99369G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.595G>T
ENST00000700557.2:n.184G>T
ENST00000700559.2:c.2092G>T	ENSP00000515065.2:p.Asp698Tyr
ENST00000546498.2:n.779G>T
ENST00000549461.2:n.631G>T
ENST00000700555.1:c.523G>T	ENSP00000515062.1:p.Asp175Tyr
ENST00000700556.1:c.563G>T
ENST00000700557.1:c.103G>T	ENSP00000515064.1:p.Asp35Tyr
ENST00000700558.1:n.306G>T
ENST00000700559.1:c.1307G>T
ENST00000700560.1:n.1307G>T
ENST00000700561.1:n.1433G>T
ENST00000070846.11:c.2224G>T	ENSP00000070846.6:p.Asp742Tyr
ENST00000340811.9:c.2092G>T MANE Select	ENSP00000342800.5:p.Asp698Tyr
ENST00000070846.10:c.2224G>T	ENSP00000070846.6:p.Asp742Tyr
ENST00000340811.8:c.2092G>T	ENSP00000342800.4:p.Asp698Tyr
ENST00000549461.1:n.538G>T
ENST00000613243.1:c.2224G>T	ENSP00000478295.1:p.Asp742Tyr
NM_001005242.2:c.2092G>T	NP_001005242.2:p.Asp698Tyr
NM_004572.3:c.2224G>T , LRG_398t1:c.2224G>T	NP_004563.2:p.Asp742Tyr
NM_001005242.3:c.2092G>T MANE Select	NP_001005242.2:p.Asp698Tyr
NM_004572.4:c.2224G>T	NP_004563.2:p.Asp742Tyr