Canonical Allele Identifier: CA1241017137
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070684_29070687delinsGTCC , CM000664.2:g.29070684_29070687delinsGTCC GRCh38
NC_000002.11:g.29293550_29293553delinsGTCC , CM000664.1:g.29293550_29293553delinsGTCC GRCh37
NC_000002.10:g.29147054_29147057delinsGTCC NCBI36
NG_021427.1:g.8575_8578delinsGGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3575_3578delinsGGAC MANE Select ENSP00000332809.4:p.Arg1192=
ENST00000331664.5:c.3575_3578delinsGGAC ENSP00000332809.4:p.Arg1192=
NM_001029883.2:c.3575_3578delinsGGAC NP_001025054.1:p.Arg1192=
XM_011532826.1:c.3575_3578delinsGGAC XP_011531128.1:p.Arg1192=
XR_939901.1:n.185+1517_185+1520delinsGTCC
XR_939902.1:n.173+1529_173+1532delinsGTCC
NM_001029883.3:c.3575_3578delinsGGAC MANE Select NP_001025054.1:p.Arg1192=
Search 100 bp 5'
Search 100 bp 3'