Canonical Allele Identifier: CA1241018934

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29072924T= , CM000664.2:g.29072924T=	GRCh38
NC_000002.11:g.29295790T= , CM000664.1:g.29295790T=	GRCh37
NC_000002.10:g.29149294T=	NCBI36
NG_021427.1:g.6338A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1338A= MANE Select	ENSP00000332809.4:p.Pro446=
ENST00000331664.5:c.1338A=	ENSP00000332809.4:p.Pro446=
NM_001029883.2:c.1338A=	NP_001025054.1:p.Pro446=
XM_011532826.1:c.1338A=	XP_011531128.1:p.Pro446=
XR_939901.1:n.185+3757T=
XR_939902.1:n.173+3769T=
NM_001029883.3:c.1338A= MANE Select	NP_001025054.1:p.Pro446=