Canonical Allele Identifier: CA1241019001
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29073057A= , CM000664.2:g.29073057A= GRCh38
NC_000002.11:g.29295923A= , CM000664.1:g.29295923A= GRCh37
NC_000002.10:g.29149427A= NCBI36
NG_021427.1:g.6205T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1205T= MANE Select ENSP00000332809.4:p.Phe402=
ENST00000331664.5:c.1205T= ENSP00000332809.4:p.Phe402=
NM_001029883.2:c.1205T= NP_001025054.1:p.Phe402=
XM_011532826.1:c.1205T= XP_011531128.1:p.Phe402=
XR_939901.1:n.185+3890A=
XR_939902.1:n.173+3902A=
NM_001029883.3:c.1205T= MANE Select NP_001025054.1:p.Phe402=