Canonical Allele Identifier: CA384364757

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32977028A>G (hg19) ; chr12:g.32824094A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32824094A>G , CM000674.2:g.32824094A>G	GRCh38
NC_000012.11:g.32977028A>G , CM000674.1:g.32977028A>G	GRCh37
NC_000012.10:g.32868295A>G	NCBI36
NG_009000.1:g.77753T>C , LRG_398:g.77753T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.137T>C
ENST00000700559.2:c.1625T>C	ENSP00000515065.2:p.Leu542Pro
ENST00000700563.2:c.1625T>C	ENSP00000515066.2:p.Leu542Pro
ENST00000546498.2:n.312T>C
ENST00000700555.1:c.65T>C	ENSP00000515062.1:p.Leu22Pro
ENST00000700556.1:c.96T>C
ENST00000700559.1:c.840T>C
ENST00000700560.1:n.840T>C
ENST00000700561.1:n.966T>C
ENST00000700563.1:c.1579T>C
ENST00000700564.1:n.1629T>C
ENST00000070846.11:c.1757T>C	ENSP00000070846.6:p.Leu586Pro
ENST00000340811.9:c.1625T>C MANE Select	ENSP00000342800.5:p.Leu542Pro
ENST00000070846.10:c.1757T>C	ENSP00000070846.6:p.Leu586Pro
ENST00000340811.8:c.1625T>C	ENSP00000342800.4:p.Leu542Pro
ENST00000546498.1:n.312T>C
ENST00000552612.5:n.46T>C
ENST00000613243.1:c.1757T>C	ENSP00000478295.1:p.Leu586Pro
NM_001005242.2:c.1625T>C	NP_001005242.2:p.Leu542Pro
NM_004572.3:c.1757T>C , LRG_398t1:c.1757T>C	NP_004563.2:p.Leu586Pro
NM_001005242.3:c.1625T>C MANE Select	NP_001005242.2:p.Leu542Pro
NM_004572.4:c.1757T>C	NP_004563.2:p.Leu586Pro