Canonical Allele Identifier: CA384359660

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32955405C>G (hg19) ; chr12:g.32802471C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32802471C>G , CM000674.2:g.32802471C>G	GRCh38
NC_000012.11:g.32955405C>G , CM000674.1:g.32955405C>G	GRCh37
NC_000012.10:g.32846672C>G	NCBI36
NG_009000.1:g.99376G>C , LRG_398:g.99376G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.602G>C
ENST00000700557.2:n.191G>C
ENST00000700559.2:c.2099G>C	ENSP00000515065.2:p.Ser700Thr
ENST00000546498.2:n.786G>C
ENST00000549461.2:n.638G>C
ENST00000700555.1:c.530G>C	ENSP00000515062.1:p.Ser177Thr
ENST00000700556.1:c.570G>C
ENST00000700557.1:c.110G>C	ENSP00000515064.1:p.Ser37Thr
ENST00000700558.1:n.313G>C
ENST00000700559.1:c.1314G>C
ENST00000700560.1:n.1314G>C
ENST00000700561.1:n.1440G>C
ENST00000070846.11:c.2231G>C	ENSP00000070846.6:p.Ser744Thr
ENST00000340811.9:c.2099G>C MANE Select	ENSP00000342800.5:p.Ser700Thr
ENST00000070846.10:c.2231G>C	ENSP00000070846.6:p.Ser744Thr
ENST00000340811.8:c.2099G>C	ENSP00000342800.4:p.Ser700Thr
ENST00000549461.1:n.545G>C
ENST00000613243.1:c.2231G>C	ENSP00000478295.1:p.Ser744Thr
NM_001005242.2:c.2099G>C	NP_001005242.2:p.Ser700Thr
NM_004572.3:c.2231G>C , LRG_398t1:c.2231G>C	NP_004563.2:p.Ser744Thr
NM_001005242.3:c.2099G>C MANE Select	NP_001005242.2:p.Ser700Thr
NM_004572.4:c.2231G>C	NP_004563.2:p.Ser744Thr