Canonical Allele Identifier: CA1241017983
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071161A= , CM000664.2:g.29071161A= GRCh38
NC_000002.11:g.29294027A= , CM000664.1:g.29294027A= GRCh37
NC_000002.10:g.29147531A= NCBI36
NG_021427.1:g.8101T=

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3101T= MANE Select ENSP00000332809.4:p.Val1034=
ENST00000331664.5:c.3101T= ENSP00000332809.4:p.Val1034=
NM_001029883.2:c.3101T= NP_001025054.1:p.Val1034=
XM_011532826.1:c.3101T= XP_011531128.1:p.Val1034=
XR_939901.1:n.185+1994A=
XR_939902.1:n.173+2006A=
NM_001029883.3:c.3101T= MANE Select NP_001025054.1:p.Val1034=