Canonical Allele Identifier: CA1241017882

Gene: PCARE

Linked Data

• dbSNP Id: rs1667468002

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29071031del , CM000664.2:g.29071031del	GRCh38
NC_000002.11:g.29293897del , CM000664.1:g.29293897del	GRCh37
NC_000002.10:g.29147401del	NCBI36
NG_021427.1:g.8233del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3233del MANE Select	ENSP00000332809.4:p.Pro1078GlnfsTer?
ENST00000331664.5:c.3233del	ENSP00000332809.4:p.Pro1078GlnfsTer?
NM_001029883.2:c.3233del	NP_001025054.1:p.Pro1078GlnfsTer?
XM_011532826.1:c.3233del	XP_011531128.1:p.Pro1078GlnfsTer?
XR_939901.1:n.185+1864del
XR_939902.1:n.173+1876del
NM_001029883.3:c.3233del MANE Select	NP_001025054.1:p.Pro1078GlnfsTer?