Canonical Allele Identifier: CA1591947
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs754173195
gnomAD v2: 2-29293726-T-G
gnomAD v3: 2-29070860-T-G
gnomAD v4: 2-29070860-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070860T>G , CM000664.2:g.29070860T>G GRCh38
NC_000002.11:g.29293726T>G , CM000664.1:g.29293726T>G GRCh37
NC_000002.10:g.29147230T>G NCBI36
NG_021427.1:g.8402A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3402A>C MANE Select ENSP00000332809.4:p.Lys1134Asn
ENST00000331664.5:c.3402A>C ENSP00000332809.4:p.Lys1134Asn
NM_001029883.2:c.3402A>C NP_001025054.1:p.Lys1134Asn
XM_011532826.1:c.3402A>C XP_011531128.1:p.Lys1134Asn
XR_939901.1:n.185+1693T>G
XR_939902.1:n.173+1705T>G
NM_001029883.3:c.3402A>C MANE Select NP_001025054.1:p.Lys1134Asn