Canonical Allele Identifier: CA1241011804

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29062398G= , CM000664.2:g.29062398G=	GRCh38
NC_000002.11:g.29285264G= , CM000664.1:g.29285264G=	GRCh37
NC_000002.10:g.29138768G=	NCBI36
NG_021427.1:g.16864C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.*2471C= MANE Select	ENSP00000332809.4:n.*2471C=
ENST00000331664.5:c.6338C=	ENSP00000332809.4:n.6338C=
NM_001029883.2:c.6338C=	NP_001025054.1:n.6338C=
XM_011532826.1:c.*382-743C=	XP_011531128.1:n.*382-743C=
NM_001029883.3:c.*2471C= MANE Select	NP_001025054.1:n.*2471C=