Canonical Allele Identifier: CA1241017981
Gene: PCARE HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071158C= , CM000664.2:g.29071158C= GRCh38
NC_000002.11:g.29294024C= , CM000664.1:g.29294024C= GRCh37
NC_000002.10:g.29147528C= NCBI36
NG_021427.1:g.8104G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3104G= MANE Select ENSP00000332809.4:p.Ser1035=
ENST00000331664.5:c.3104G= ENSP00000332809.4:p.Ser1035=
NM_001029883.2:c.3104G= NP_001025054.1:p.Ser1035=
XM_011532826.1:c.3104G= XP_011531128.1:p.Ser1035=
XR_939901.1:n.185+1991C=
XR_939902.1:n.173+2003C=
NM_001029883.3:c.3104G= MANE Select NP_001025054.1:p.Ser1035=
Search 100 bp 5'
Search 100 bp 3'