Canonical Allele Identifier: CA346475050
Gene: PCARE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070865C>A , CM000664.2:g.29070865C>A GRCh38
NC_000002.11:g.29293731C>A , CM000664.1:g.29293731C>A GRCh37
NC_000002.10:g.29147235C>A NCBI36
NG_021427.1:g.8397G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3397G>T MANE Select ENSP00000332809.4:p.Ala1133Ser
ENST00000331664.5:c.3397G>T ENSP00000332809.4:p.Ala1133Ser
NM_001029883.2:c.3397G>T NP_001025054.1:p.Ala1133Ser
XM_011532826.1:c.3397G>T XP_011531128.1:p.Ala1133Ser
XR_939901.1:n.185+1698C>A
XR_939902.1:n.173+1710C>A
NM_001029883.3:c.3397G>T MANE Select NP_001025054.1:p.Ala1133Ser