Canonical Allele Identifier: CA1241013391

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29073103G= , CM000664.2:g.29073103G=	GRCh38
NC_000002.11:g.29295969G= , CM000664.1:g.29295969G=	GRCh37
NC_000002.10:g.29149473G=	NCBI36
NG_021427.1:g.6159C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1159C= MANE Select	ENSP00000332809.4:p.His387=
ENST00000331664.5:c.1159C=	ENSP00000332809.4:p.His387=
NM_001029883.2:c.1159C=	NP_001025054.1:p.His387=
XM_011532826.1:c.1159C=	XP_011531128.1:p.His387=
XR_939901.1:n.185+3936G=
XR_939902.1:n.173+3948G=
NM_001029883.3:c.1159C= MANE Select	NP_001025054.1:p.His387=