Canonical Allele Identifier: CA44639369

Gene: PCARE

Linked Data

• dbSNP Id: rs35947026

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29070793dup , CM000664.2:g.29070793dup	GRCh38
NC_000002.11:g.29293659dup , CM000664.1:g.29293659dup	GRCh37
NC_000002.10:g.29147163dup	NCBI36
NG_021427.1:g.8471dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3471dup MANE Select	ENSP00000332809.4:p.Asn1158GlufsTer?
ENST00000331664.5:c.3471dup	ENSP00000332809.4:p.Asn1158GlufsTer?
NM_001029883.2:c.3471dup	NP_001025054.1:p.Asn1158GlufsTer?
XM_011532826.1:c.3471dup	XP_011531128.1:p.Asn1158GlufsTer?
XR_939901.1:n.185+1626dup
XR_939902.1:n.173+1638dup
NM_001029883.3:c.3471dup MANE Select	NP_001025054.1:p.Asn1158GlufsTer?