Canonical Allele Identifier: CA1241013389

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29073102T= , CM000664.2:g.29073102T=	GRCh38
NC_000002.11:g.29295968T= , CM000664.1:g.29295968T=	GRCh37
NC_000002.10:g.29149472T=	NCBI36
NG_021427.1:g.6160A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1160A= MANE Select	ENSP00000332809.4:p.His387=
ENST00000331664.5:c.1160A=	ENSP00000332809.4:p.His387=
NM_001029883.2:c.1160A=	NP_001025054.1:p.His387=
XM_011532826.1:c.1160A=	XP_011531128.1:p.His387=
XR_939901.1:n.185+3935T=
XR_939902.1:n.173+3947T=
NM_001029883.3:c.1160A= MANE Select	NP_001025054.1:p.His387=