Canonical Allele Identifier: CA384359165

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32955340T>G (hg19) ; chr12:g.32802406T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32802406T>G , CM000674.2:g.32802406T>G	GRCh38
NC_000012.11:g.32955340T>G , CM000674.1:g.32955340T>G	GRCh37
NC_000012.10:g.32846607T>G	NCBI36
NG_009000.1:g.99441A>C , LRG_398:g.99441A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.667A>C
ENST00000700557.2:n.256A>C
ENST00000700559.2:c.2164A>C	ENSP00000515065.2:p.Ile722Leu
ENST00000546498.2:n.851A>C
ENST00000549461.2:n.659+44A>C
ENST00000700555.1:c.595A>C	ENSP00000515062.1:p.Ile199Leu
ENST00000700556.1:c.635A>C
ENST00000700557.1:c.175A>C	ENSP00000515064.1:p.Ile59Leu
ENST00000700558.1:n.378A>C
ENST00000700559.1:c.1379A>C
ENST00000700560.1:n.1379A>C
ENST00000700561.1:n.1505A>C
ENST00000070846.11:c.2296A>C	ENSP00000070846.6:p.Ile766Leu
ENST00000340811.9:c.2164A>C MANE Select	ENSP00000342800.5:p.Ile722Leu
ENST00000070846.10:c.2296A>C	ENSP00000070846.6:p.Ile766Leu
ENST00000340811.8:c.2164A>C	ENSP00000342800.4:p.Ile722Leu
ENST00000613243.1:c.2296A>C	ENSP00000478295.1:p.Ile766Leu
NM_001005242.2:c.2164A>C	NP_001005242.2:p.Ile722Leu
NM_004572.3:c.2296A>C , LRG_398t1:c.2296A>C	NP_004563.2:p.Ile766Leu
NM_001005242.3:c.2164A>C MANE Select	NP_001005242.2:p.Ile722Leu
NM_004572.4:c.2296A>C	NP_004563.2:p.Ile766Leu