Canonical Allele Identifier: CA1241017186

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29070721G= , CM000664.2:g.29070721G=	GRCh38
NC_000002.11:g.29293587G= , CM000664.1:g.29293587G=	GRCh37
NC_000002.10:g.29147091G=	NCBI36
NG_021427.1:g.8541C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3541C= MANE Select	ENSP00000332809.4:p.Leu1181=
ENST00000331664.5:c.3541C=	ENSP00000332809.4:p.Leu1181=
NM_001029883.2:c.3541C=	NP_001025054.1:p.Leu1181=
XM_011532826.1:c.3541C=	XP_011531128.1:p.Leu1181=
XR_939901.1:n.185+1554G=
XR_939902.1:n.173+1566G=
NM_001029883.3:c.3541C= MANE Select	NP_001025054.1:p.Leu1181=