Canonical Allele Identifier: CA1241019002
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29073063C= , CM000664.2:g.29073063C= GRCh38
NC_000002.11:g.29295929C= , CM000664.1:g.29295929C= GRCh37
NC_000002.10:g.29149433C= NCBI36
NG_021427.1:g.6199G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1199G= MANE Select ENSP00000332809.4:p.Ser400=
ENST00000331664.5:c.1199G= ENSP00000332809.4:p.Ser400=
NM_001029883.2:c.1199G= NP_001025054.1:p.Ser400=
XM_011532826.1:c.1199G= XP_011531128.1:p.Ser400=
XR_939901.1:n.185+3896C=
XR_939902.1:n.173+3908C=
NM_001029883.3:c.1199G= MANE Select NP_001025054.1:p.Ser400=