Canonical Allele Identifier: CA1241017838
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071013_29071015delinsAGG , CM000664.2:g.29071013_29071015delinsAGG GRCh38
NC_000002.11:g.29293879_29293881delinsAGG , CM000664.1:g.29293879_29293881delinsAGG GRCh37
NC_000002.10:g.29147383_29147385delinsAGG NCBI36
NG_021427.1:g.8247_8249delinsCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3247_3249delinsCCT MANE Select ENSP00000332809.4:p.Pro1083=
ENST00000331664.5:c.3247_3249delinsCCT ENSP00000332809.4:p.Pro1083=
NM_001029883.2:c.3247_3249delinsCCT NP_001025054.1:p.Pro1083=
XM_011532826.1:c.3247_3249delinsCCT XP_011531128.1:p.Pro1083=
XR_939901.1:n.185+1846_185+1848delinsAGG
XR_939902.1:n.173+1858_173+1860delinsAGG
NM_001029883.3:c.3247_3249delinsCCT MANE Select NP_001025054.1:p.Pro1083=
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