Canonical Allele Identifier: CA916500199
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs1553354365
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071039_29071040delinsGG , CM000664.2:g.29071039_29071040delinsGG GRCh38
NC_000002.11:g.29293905_29293906delinsGG , CM000664.1:g.29293905_29293906delinsGG GRCh37
NC_000002.10:g.29147409_29147410delinsGG NCBI36
NG_021427.1:g.8222_8223delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3222_3223delinsCC MANE Select ENSP00000332809.4:p.Thr1075Pro
ENST00000331664.5:c.3222_3223delinsCC ENSP00000332809.4:p.Thr1075Pro
NM_001029883.2:c.3222_3223delinsCC NP_001025054.1:p.Thr1075Pro
XM_011532826.1:c.3222_3223delinsCC XP_011531128.1:p.Thr1075Pro
XR_939901.1:n.185+1872_185+1873delinsGG
XR_939902.1:n.173+1884_173+1885delinsGG
NM_001029883.3:c.3222_3223delinsCC MANE Select NP_001025054.1:p.Thr1075Pro
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