Canonical Allele Identifier: CA1241017889

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29071032T= , CM000664.2:g.29071032T=	GRCh38
NC_000002.11:g.29293898T= , CM000664.1:g.29293898T=	GRCh37
NC_000002.10:g.29147402T=	NCBI36
NG_021427.1:g.8230A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3230A= MANE Select	ENSP00000332809.4:p.His1077=
ENST00000331664.5:c.3230A=	ENSP00000332809.4:p.His1077=
NM_001029883.2:c.3230A=	NP_001025054.1:p.His1077=
XM_011532826.1:c.3230A=	XP_011531128.1:p.His1077=
XR_939901.1:n.185+1865T=
XR_939902.1:n.173+1877T=
NM_001029883.3:c.3230A= MANE Select	NP_001025054.1:p.His1077=