Canonical Allele Identifier: CA1241017312
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070772_29070773delinsTC , CM000664.2:g.29070772_29070773delinsTC GRCh38
NC_000002.11:g.29293638_29293639delinsTC , CM000664.1:g.29293638_29293639delinsTC GRCh37
NC_000002.10:g.29147142_29147143delinsTC NCBI36
NG_021427.1:g.8489_8490delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3489_3490delinsGA MANE Select ENSP00000332809.4:p.Trp1163=
ENST00000331664.5:c.3489_3490delinsGA ENSP00000332809.4:p.Trp1163=
NM_001029883.2:c.3489_3490delinsGA NP_001025054.1:p.Trp1163=
XM_011532826.1:c.3489_3490delinsGA XP_011531128.1:p.Trp1163=
XR_939901.1:n.185+1605_185+1606delinsTC
XR_939902.1:n.173+1617_173+1618delinsTC
NM_001029883.3:c.3489_3490delinsGA MANE Select NP_001025054.1:p.Trp1163=
Search 100 bp 5'
Search 100 bp 3'