Canonical Allele Identifier: CA1241013378

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29073097C= , CM000664.2:g.29073097C=	GRCh38
NC_000002.11:g.29295963C= , CM000664.1:g.29295963C=	GRCh37
NC_000002.10:g.29149467C=	NCBI36
NG_021427.1:g.6165G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1165G= MANE Select	ENSP00000332809.4:p.Glu389=
ENST00000331664.5:c.1165G=	ENSP00000332809.4:p.Glu389=
NM_001029883.2:c.1165G=	NP_001025054.1:p.Glu389=
XM_011532826.1:c.1165G=	XP_011531128.1:p.Glu389=
XR_939901.1:n.185+3930C=
XR_939902.1:n.173+3942C=
NM_001029883.3:c.1165G= MANE Select	NP_001025054.1:p.Glu389=