Canonical Allele Identifier: CA425616666

Gene: PCARE

Linked Data

• MyVariant Identifiers: chr2:g.29293789G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29070923G>T , CM000664.2:g.29070923G>T	GRCh38
NC_000002.11:g.29293789G>T , CM000664.1:g.29293789G>T	GRCh37
NC_000002.10:g.29147293G>T	NCBI36
NG_021427.1:g.8339C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3339C>A MANE Select	ENSP00000332809.4:p.Ala1113=
ENST00000331664.5:c.3339C>A	ENSP00000332809.4:p.Ala1113=
NM_001029883.2:c.3339C>A	NP_001025054.1:p.Ala1113=
XM_011532826.1:c.3339C>A	XP_011531128.1:p.Ala1113=
XR_939901.1:n.185+1756G>T
XR_939902.1:n.173+1768G>T
NM_001029883.3:c.3339C>A MANE Select	NP_001025054.1:p.Ala1113=