Canonical Allele Identifier: CA346480295
Gene: PCARE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29072872A>C , CM000664.2:g.29072872A>C GRCh38
NC_000002.11:g.29295738A>C , CM000664.1:g.29295738A>C GRCh37
NC_000002.10:g.29149242A>C NCBI36
NG_021427.1:g.6390T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1390T>G MANE Select ENSP00000332809.4:p.Ser464Ala
ENST00000331664.5:c.1390T>G ENSP00000332809.4:p.Ser464Ala
NM_001029883.2:c.1390T>G NP_001025054.1:p.Ser464Ala
XM_011532826.1:c.1390T>G XP_011531128.1:p.Ser464Ala
XR_939901.1:n.185+3705A>C
XR_939902.1:n.173+3717A>C
NM_001029883.3:c.1390T>G MANE Select NP_001025054.1:p.Ser464Ala