Canonical Allele Identifier: CA1241017284

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29070760_29070761delinsCT , CM000664.2:g.29070760_29070761delinsCT	GRCh38
NC_000002.11:g.29293626_29293627delinsCT , CM000664.1:g.29293626_29293627delinsCT	GRCh37
NC_000002.10:g.29147130_29147131delinsCT	NCBI36
NG_021427.1:g.8501_8502delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3501_3502delinsAG MANE Select	ENSP00000332809.4:p.Ser1167=
ENST00000331664.5:c.3501_3502delinsAG	ENSP00000332809.4:p.Ser1167=
NM_001029883.2:c.3501_3502delinsAG	NP_001025054.1:p.Ser1167=
XM_011532826.1:c.3501_3502delinsAG	XP_011531128.1:p.Ser1167=
XR_939901.1:n.185+1593_185+1594delinsCT
XR_939902.1:n.173+1605_173+1606delinsCT
NM_001029883.3:c.3501_3502delinsAG MANE Select	NP_001025054.1:p.Ser1167=