Canonical Allele Identifier: CA1241017925

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29071065_29071078delinsGCAGGTGCACTCTC , CM000664.2:g.29071065_29071078delinsGCAGGTGCACTCTC	GRCh38
NC_000002.11:g.29293931_29293944delinsGCAGGTGCACTCTC , CM000664.1:g.29293931_29293944delinsGCAGGTGCACTCTC	GRCh37
NC_000002.10:g.29147435_29147448delinsGCAGGTGCACTCTC	NCBI36
NG_021427.1:g.8184_8197delinsGAGAGTGCACCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3184_3197delinsGAGAGTGCACCTGC MANE Select	ENSP00000332809.4:p.Glu1062=
ENST00000331664.5:c.3184_3197delinsGAGAGTGCACCTGC	ENSP00000332809.4:p.Glu1062=
NM_001029883.2:c.3184_3197delinsGAGAGTGCACCTGC	NP_001025054.1:p.Glu1062=
XM_011532826.1:c.3184_3197delinsGAGAGTGCACCTGC	XP_011531128.1:p.Glu1062=
XR_939901.1:n.185+1898_185+1911delinsGCAGGTGCACTCTC
XR_939902.1:n.173+1910_173+1923delinsGCAGGTGCACTCTC
NM_001029883.3:c.3184_3197delinsGAGAGTGCACCTGC MANE Select	NP_001025054.1:p.Glu1062=