Canonical Allele Identifier: CA1241017998
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071187A= , CM000664.2:g.29071187A= GRCh38
NC_000002.11:g.29294053A= , CM000664.1:g.29294053A= GRCh37
NC_000002.10:g.29147557A= NCBI36
NG_021427.1:g.8075T=

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3075T= MANE Select ENSP00000332809.4:p.Ala1025=
ENST00000331664.5:c.3075T= ENSP00000332809.4:p.Ala1025=
NM_001029883.2:c.3075T= NP_001025054.1:p.Ala1025=
XM_011532826.1:c.3075T= XP_011531128.1:p.Ala1025=
XR_939901.1:n.185+2020A=
XR_939902.1:n.173+2032A=
NM_001029883.3:c.3075T= MANE Select NP_001025054.1:p.Ala1025=