Canonical Allele Identifier: CA1592458
Community Standard Title: NM_001029883.3(PCARE):c.1297C>T (p.Pro433Ser)
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29072965G>A , CM000664.2:g.29072965G>A GRCh38
NC_000002.11:g.29295831G>A , CM000664.1:g.29295831G>A GRCh37
NC_000002.10:g.29149335G>A NCBI36
NG_021427.1:g.6297C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001029883.3:c.1297C>T MANE Select NP_001025054.1:p.Pro433Ser
ENST00000331664.6:c.1297C>T MANE Select ENSP00000332809.4:p.Pro433Ser
NM_001029883.2:c.1297C>T NP_001025054.1:p.Pro433Ser
ENST00000331664.5:c.1297C>T ENSP00000332809.4:p.Pro433Ser
XM_011532826.1:c.1297C>T XP_011531128.1:p.Pro433Ser
XR_939901.1:n.185+3798G>A
XR_939902.1:n.173+3810G>A
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