Canonical Allele Identifier: CA037852

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32878338T>G , CM000674.2:g.32878338T>G	GRCh38
NC_000012.11:g.33031272T>G , CM000674.1:g.33031272T>G	GRCh37
NC_000012.10:g.32922539T>G	NCBI36
NG_009000.1:g.23509A>C , LRG_398:g.23509A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001005242.3:c.542A>C MANE Select	NP_001005242.2:p.Gln181Pro
ENST00000340811.9:c.542A>C MANE Select	ENSP00000342800.5:p.Gln181Pro
NM_001005242.2:c.542A>C	NP_001005242.2:p.Gln181Pro
NM_004572.3:c.542A>C , LRG_398t1:c.542A>C	NP_004563.2:p.Gln181Pro
NM_004572.4:c.542A>C	NP_004563.2:p.Gln181Pro
ENST00000070846.10:c.542A>C	ENSP00000070846.6:p.Gln181Pro
ENST00000070846.11:c.542A>C	ENSP00000070846.6:p.Gln181Pro
ENST00000340811.8:c.542A>C	ENSP00000342800.4:p.Gln181Pro
ENST00000613243.1:c.542A>C	ENSP00000478295.1:p.Gln181Pro
ENST00000700559.2:c.542A>C	ENSP00000515065.2:p.Gln181Pro
ENST00000700563.1:c.496A>C
ENST00000700563.2:c.542A>C	ENSP00000515066.2:p.Gln181Pro
ENST00000700564.1:n.546A>C
ENST00000700565.1:n.395A>C