Canonical Allele Identifier: CA2658450987
Gene: PCARE HGNC NCBI

Linked Data

gnomAD v4: 2-29072875-C-CCCCAAT
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29072881_29072886dup , CM000664.2:g.29072881_29072886dup GRCh38
NC_000002.11:g.29295747_29295752dup , CM000664.1:g.29295747_29295752dup GRCh37
NC_000002.10:g.29149251_29149256dup NCBI36
NG_021427.1:g.6381_6386dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1381_1386dup MANE Select ENSP00000332809.4:p.Gly462_Val463insIleGly
ENST00000331664.5:c.1381_1386dup ENSP00000332809.4:p.Gly462_Val463insIleGly
NM_001029883.2:c.1381_1386dup NP_001025054.1:p.Gly462_Val463insIleGly
XM_011532826.1:c.1381_1386dup XP_011531128.1:p.Gly462_Val463insIleGly
XR_939901.1:n.185+3714_185+3719dup
XR_939902.1:n.173+3726_173+3731dup
NM_001029883.3:c.1381_1386dup MANE Select NP_001025054.1:p.Gly462_Val463insIleGly
Search 100 bp 5'
Search 100 bp 3'