Canonical Allele Identifier: CA1241017996

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29071185A= , CM000664.2:g.29071185A=	GRCh38
NC_000002.11:g.29294051A= , CM000664.1:g.29294051A=	GRCh37
NC_000002.10:g.29147555A=	NCBI36
NG_021427.1:g.8077T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000331664.6:c.3077T= MANE Select	ENSP00000332809.4:p.Val1026=
ENST00000331664.5:c.3077T=	ENSP00000332809.4:p.Val1026=
NM_001029883.2:c.3077T=	NP_001025054.1:p.Val1026=
XM_011532826.1:c.3077T=	XP_011531128.1:p.Val1026=
XR_939901.1:n.185+2018A=
XR_939902.1:n.173+2030A=
NM_001029883.3:c.3077T= MANE Select	NP_001025054.1:p.Val1026=