Canonical Allele Identifier: CA346472887
Gene: PCARE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070694G>C , CM000664.2:g.29070694G>C GRCh38
NC_000002.11:g.29293560G>C , CM000664.1:g.29293560G>C GRCh37
NC_000002.10:g.29147064G>C NCBI36
NG_021427.1:g.8568C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3568C>G MANE Select ENSP00000332809.4:p.Leu1190Val
ENST00000331664.5:c.3568C>G ENSP00000332809.4:p.Leu1190Val
NM_001029883.2:c.3568C>G NP_001025054.1:p.Leu1190Val
XM_011532826.1:c.3568C>G XP_011531128.1:p.Leu1190Val
XR_939901.1:n.185+1527G>C
XR_939902.1:n.173+1539G>C
NM_001029883.3:c.3568C>G MANE Select NP_001025054.1:p.Leu1190Val