Canonical Allele Identifier: CA384359376

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32955372T>G (hg19) ; chr12:g.32802438T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32802438T>G , CM000674.2:g.32802438T>G	GRCh38
NC_000012.11:g.32955372T>G , CM000674.1:g.32955372T>G	GRCh37
NC_000012.10:g.32846639T>G	NCBI36
NG_009000.1:g.99409A>C , LRG_398:g.99409A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.635A>C
ENST00000700557.2:n.224A>C
ENST00000700559.2:c.2132A>C	ENSP00000515065.2:p.Asn711Thr
ENST00000546498.2:n.819A>C
ENST00000549461.2:n.659+12A>C
ENST00000700555.1:c.563A>C	ENSP00000515062.1:p.Asn188Thr
ENST00000700556.1:c.603A>C
ENST00000700557.1:c.143A>C	ENSP00000515064.1:p.Asn48Thr
ENST00000700558.1:n.346A>C
ENST00000700559.1:c.1347A>C
ENST00000700560.1:n.1347A>C
ENST00000700561.1:n.1473A>C
ENST00000070846.11:c.2264A>C	ENSP00000070846.6:p.Asn755Thr
ENST00000340811.9:c.2132A>C MANE Select	ENSP00000342800.5:p.Asn711Thr
ENST00000070846.10:c.2264A>C	ENSP00000070846.6:p.Asn755Thr
ENST00000340811.8:c.2132A>C	ENSP00000342800.4:p.Asn711Thr
ENST00000613243.1:c.2264A>C	ENSP00000478295.1:p.Asn755Thr
NM_001005242.2:c.2132A>C	NP_001005242.2:p.Asn711Thr
NM_004572.3:c.2264A>C , LRG_398t1:c.2264A>C	NP_004563.2:p.Asn755Thr
NM_001005242.3:c.2132A>C MANE Select	NP_001005242.2:p.Asn711Thr
NM_004572.4:c.2264A>C	NP_004563.2:p.Asn755Thr