Canonical Allele Identifier: CA1241018067

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29071299G= , CM000664.2:g.29071299G=	GRCh38
NC_000002.11:g.29294165G= , CM000664.1:g.29294165G=	GRCh37
NC_000002.10:g.29147669G=	NCBI36
NG_021427.1:g.7963C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.2963C= MANE Select	ENSP00000332809.4:p.Pro988=
ENST00000331664.5:c.2963C=	ENSP00000332809.4:p.Pro988=
NM_001029883.2:c.2963C=	NP_001025054.1:p.Pro988=
XM_011532826.1:c.2963C=	XP_011531128.1:p.Pro988=
XR_939901.1:n.185+2132G=
XR_939902.1:n.173+2144G=
NM_001029883.3:c.2963C= MANE Select	NP_001025054.1:p.Pro988=