Canonical Allele Identifier: CA2658449605
Gene: PCARE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071054_29071091del , CM000664.2:g.29071054_29071091del GRCh38
NC_000002.11:g.29293920_29293957del , CM000664.1:g.29293920_29293957del GRCh37
NC_000002.10:g.29147424_29147461del NCBI36
NG_021427.1:g.8171_8208del

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3171_3208del MANE Select ENSP00000332809.4:p.Asn1058ProfsTer?
ENST00000331664.5:c.3171_3208del ENSP00000332809.4:p.Asn1058ProfsTer?
NM_001029883.2:c.3171_3208del NP_001025054.1:p.Asn1058ProfsTer?
XM_011532826.1:c.3171_3208del XP_011531128.1:p.Asn1058ProfsTer?
XR_939901.1:n.185+1887_185+1924del
XR_939902.1:n.173+1899_173+1936del
NM_001029883.3:c.3171_3208del MANE Select NP_001025054.1:p.Asn1058ProfsTer?