Canonical Allele Identifier: CA1241017922
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs1667468990
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071054_29071055insACACATTCCATATT , CM000664.2:g.29071054_29071055insACACATTCCATATT GRCh38
NC_000002.11:g.29293920_29293921insACACATTCCATATT , CM000664.1:g.29293920_29293921insACACATTCCATATT GRCh37
NC_000002.10:g.29147424_29147425insACACATTCCATATT NCBI36
NG_021427.1:g.8207_8208insAATATGGAATGTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3207_3208insAATATGGAATGTGT MANE Select ENSP00000332809.4:p.Val1070AsnfsTer?
ENST00000331664.5:c.3207_3208insAATATGGAATGTGT ENSP00000332809.4:p.Val1070AsnfsTer?
NM_001029883.2:c.3207_3208insAATATGGAATGTGT NP_001025054.1:p.Val1070AsnfsTer?
XM_011532826.1:c.3207_3208insAATATGGAATGTGT XP_011531128.1:p.Val1070AsnfsTer?
XR_939901.1:n.185+1887_185+1888insACACATTCCATATT
XR_939902.1:n.173+1899_173+1900insACACATTCCATATT
NM_001029883.3:c.3207_3208insAATATGGAATGTGT MANE Select NP_001025054.1:p.Val1070AsnfsTer?
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