Canonical Allele Identifier: CA1241018912
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29072884_29072885delinsCA , CM000664.2:g.29072884_29072885delinsCA GRCh38
NC_000002.11:g.29295750_29295751delinsCA , CM000664.1:g.29295750_29295751delinsCA GRCh37
NC_000002.10:g.29149254_29149255delinsCA NCBI36
NG_021427.1:g.6377_6378delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1377_1378delinsTG MANE Select ENSP00000332809.4:p.Phe459=
ENST00000331664.5:c.1377_1378delinsTG ENSP00000332809.4:p.Phe459=
NM_001029883.2:c.1377_1378delinsTG NP_001025054.1:p.Phe459=
XM_011532826.1:c.1377_1378delinsTG XP_011531128.1:p.Phe459=
XR_939901.1:n.185+3717_185+3718delinsCA
XR_939902.1:n.173+3729_173+3730delinsCA
NM_001029883.3:c.1377_1378delinsTG MANE Select NP_001025054.1:p.Phe459=
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