Canonical Allele Identifier: CA346480344

Gene: PCARE

Linked Data

• MyVariant Identifiers: chr2:g.29295762A>T (hg19) ; chr2:g.29072896A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29072896A>T , CM000664.2:g.29072896A>T	GRCh38
NC_000002.11:g.29295762A>T , CM000664.1:g.29295762A>T	GRCh37
NC_000002.10:g.29149266A>T	NCBI36
NG_021427.1:g.6366T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1366T>A MANE Select	ENSP00000332809.4:p.Cys456Ser
ENST00000331664.5:c.1366T>A	ENSP00000332809.4:p.Cys456Ser
NM_001029883.2:c.1366T>A	NP_001025054.1:p.Cys456Ser
XM_011532826.1:c.1366T>A	XP_011531128.1:p.Cys456Ser
XR_939901.1:n.185+3729A>T
XR_939902.1:n.173+3741A>T
NM_001029883.3:c.1366T>A MANE Select	NP_001025054.1:p.Cys456Ser