Canonical Allele Identifier: CA1241018905

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29072875C= , CM000664.2:g.29072875C=	GRCh38
NC_000002.11:g.29295741C= , CM000664.1:g.29295741C=	GRCh37
NC_000002.10:g.29149245C=	NCBI36
NG_021427.1:g.6387G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1387G= MANE Select	ENSP00000332809.4:p.Val463=
ENST00000331664.5:c.1387G=	ENSP00000332809.4:p.Val463=
NM_001029883.2:c.1387G=	NP_001025054.1:p.Val463=
XM_011532826.1:c.1387G=	XP_011531128.1:p.Val463=
XR_939901.1:n.185+3708C=
XR_939902.1:n.173+3720C=
NM_001029883.3:c.1387G= MANE Select	NP_001025054.1:p.Val463=