Canonical Allele Identifier: CA1241017192
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070723_29070741delinsGCTGCTCTCCGCTGCGAGT , CM000664.2:g.29070723_29070741delinsGCTGCTCTCCGCTGCGAGT GRCh38
NC_000002.11:g.29293589_29293607delinsGCTGCTCTCCGCTGCGAGT , CM000664.1:g.29293589_29293607delinsGCTGCTCTCCGCTGCGAGT GRCh37
NC_000002.10:g.29147093_29147111delinsGCTGCTCTCCGCTGCGAGT NCBI36
NG_021427.1:g.8521_8539delinsACTCGCAGCGGAGAGCAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3521_3539delinsACTCGCAGCGGAGAGCAGC MANE Select ENSP00000332809.4:p.Asp1174=
ENST00000331664.5:c.3521_3539delinsACTCGCAGCGGAGAGCAGC ENSP00000332809.4:p.Asp1174=
NM_001029883.2:c.3521_3539delinsACTCGCAGCGGAGAGCAGC NP_001025054.1:p.Asp1174=
XM_011532826.1:c.3521_3539delinsACTCGCAGCGGAGAGCAGC XP_011531128.1:p.Asp1174=
XR_939901.1:n.185+1556_185+1574delinsGCTGCTCTCCGCTGCGAGT
XR_939902.1:n.173+1568_173+1586delinsGCTGCTCTCCGCTGCGAGT
NM_001029883.3:c.3521_3539delinsACTCGCAGCGGAGAGCAGC MANE Select NP_001025054.1:p.Asp1174=
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