Canonical Allele Identifier: CA1241018022

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29071233C= , CM000664.2:g.29071233C=	GRCh38
NC_000002.11:g.29294099C= , CM000664.1:g.29294099C=	GRCh37
NC_000002.10:g.29147603C=	NCBI36
NG_021427.1:g.8029G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3029G= MANE Select	ENSP00000332809.4:p.Arg1010=
ENST00000331664.5:c.3029G=	ENSP00000332809.4:p.Arg1010=
NM_001029883.2:c.3029G=	NP_001025054.1:p.Arg1010=
XM_011532826.1:c.3029G=	XP_011531128.1:p.Arg1010=
XR_939901.1:n.185+2066C=
XR_939902.1:n.173+2078C=
NM_001029883.3:c.3029G= MANE Select	NP_001025054.1:p.Arg1010=