Canonical Allele Identifier: CA2576924629
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29072878dup , CM000664.2:g.29072878dup GRCh38
NC_000002.11:g.29295744dup , CM000664.1:g.29295744dup GRCh37
NC_000002.10:g.29149248dup NCBI36
NG_021427.1:g.6387dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1387dup MANE Select ENSP00000332809.4:p.Val463GlyfsTer20
ENST00000331664.5:c.1387dup ENSP00000332809.4:p.Val463GlyfsTer20
NM_001029883.2:c.1387dup NP_001025054.1:p.Val463GlyfsTer20
XM_011532826.1:c.1387dup XP_011531128.1:p.Val463GlyfsTer20
XR_939901.1:n.185+3711dup
XR_939902.1:n.173+3723dup
NM_001029883.3:c.1387dup MANE Select NP_001025054.1:p.Val463GlyfsTer20
Search 100 bp 5'
Search 100 bp 3'