Canonical Allele Identifier: CA384357578

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32949072C>A (hg19) ; chr12:g.32796138C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32796138C>A , CM000674.2:g.32796138C>A	GRCh38
NC_000012.11:g.32949072C>A , CM000674.1:g.32949072C>A	GRCh37
NC_000012.10:g.32840339C>A	NCBI36
NG_009000.1:g.105709G>T , LRG_398:g.105709G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.831G>T
ENST00000700557.2:n.420G>T
ENST00000700559.2:c.2168-3407G>T	ENSP00000515065.2:n.2168-3407G>T
ENST00000546498.2:n.1015G>T
ENST00000549461.2:n.820G>T
ENST00000700555.1:c.759G>T	ENSP00000515062.1:p.Gln253His
ENST00000700556.1:c.799G>T
ENST00000700557.1:c.339G>T	ENSP00000515064.1:p.Gln113His
ENST00000700558.1:n.542G>T
ENST00000700559.1:c.1383-3407G>T
ENST00000700560.1:n.1543G>T
ENST00000700561.1:n.1669G>T
ENST00000070846.11:c.2460G>T	ENSP00000070846.6:p.Gln820His
ENST00000340811.9:c.2328G>T MANE Select	ENSP00000342800.5:p.Gln776His
ENST00000070846.10:c.2460G>T	ENSP00000070846.6:p.Gln820His
ENST00000340811.8:c.2328G>T	ENSP00000342800.4:p.Gln776His
ENST00000613243.1:c.2458G>T	ENSP00000478295.1:p.Glu820Ter
NM_001005242.2:c.2328G>T	NP_001005242.2:p.Gln776His
NM_004572.3:c.2460G>T , LRG_398t1:c.2460G>T	NP_004563.2:p.Gln820His
NM_001005242.3:c.2328G>T MANE Select	NP_001005242.2:p.Gln776His
NM_004572.4:c.2460G>T	NP_004563.2:p.Gln820His