Canonical Allele Identifier: CA2658450993

Gene: PCARE

Linked Data

• gnomAD v4: 2-29073102-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29073106dup , CM000664.2:g.29073106dup	GRCh38
NC_000002.11:g.29295972dup , CM000664.1:g.29295972dup	GRCh37
NC_000002.10:g.29149476dup	NCBI36
NG_021427.1:g.6159dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1159dup MANE Select	ENSP00000332809.4:p.His387ProfsTer?
ENST00000331664.5:c.1159dup	ENSP00000332809.4:p.His387ProfsTer?
NM_001029883.2:c.1159dup	NP_001025054.1:p.His387ProfsTer?
XM_011532826.1:c.1159dup	XP_011531128.1:p.His387ProfsTer?
XR_939901.1:n.185+3939dup
XR_939902.1:n.173+3951dup
NM_001029883.3:c.1159dup MANE Select	NP_001025054.1:p.His387ProfsTer?