Canonical Allele Identifier: CA1241018929
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29072914G= , CM000664.2:g.29072914G= GRCh38
NC_000002.11:g.29295780G= , CM000664.1:g.29295780G= GRCh37
NC_000002.10:g.29149284G= NCBI36
NG_021427.1:g.6348C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1348C= MANE Select ENSP00000332809.4:p.Leu450=
ENST00000331664.5:c.1348C= ENSP00000332809.4:p.Leu450=
NM_001029883.2:c.1348C= NP_001025054.1:p.Leu450=
XM_011532826.1:c.1348C= XP_011531128.1:p.Leu450=
XR_939901.1:n.185+3747G=
XR_939902.1:n.173+3759G=
NM_001029883.3:c.1348C= MANE Select NP_001025054.1:p.Leu450=
Search 100 bp 5'
Search 100 bp 3'