Canonical Allele Identifier: CA1241013449

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29073136C= , CM000664.2:g.29073136C=	GRCh38
NC_000002.11:g.29296002C= , CM000664.1:g.29296002C=	GRCh37
NC_000002.10:g.29149506C=	NCBI36
NG_021427.1:g.6126G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1126G= MANE Select	ENSP00000332809.4:p.Glu376=
ENST00000331664.5:c.1126G=	ENSP00000332809.4:p.Glu376=
NM_001029883.2:c.1126G=	NP_001025054.1:p.Glu376=
XM_011532826.1:c.1126G=	XP_011531128.1:p.Glu376=
XR_939901.1:n.185+3969C=
XR_939902.1:n.173+3981C=
NM_001029883.3:c.1126G= MANE Select	NP_001025054.1:p.Glu376=