Canonical Allele Identifier: CA1241018039

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29071260C= , CM000664.2:g.29071260C=	GRCh38
NC_000002.11:g.29294126C= , CM000664.1:g.29294126C=	GRCh37
NC_000002.10:g.29147630C=	NCBI36
NG_021427.1:g.8002G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3002G= MANE Select	ENSP00000332809.4:p.Trp1001=
ENST00000331664.5:c.3002G=	ENSP00000332809.4:p.Trp1001=
NM_001029883.2:c.3002G=	NP_001025054.1:p.Trp1001=
XM_011532826.1:c.3002G=	XP_011531128.1:p.Trp1001=
XR_939901.1:n.185+2093C=
XR_939902.1:n.173+2105C=
NM_001029883.3:c.3002G= MANE Select	NP_001025054.1:p.Trp1001=