Canonical Allele Identifier: CA361219585
Gene: PCDHA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.140166963C>A (hg19) chr5:g.140787378C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140787378C>A , CM000667.2:g.140787378C>A GRCh38
NC_000005.9:g.140166963C>A , CM000667.1:g.140166963C>A GRCh37
NC_000005.8:g.140147147C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504120.4:c.1088C>A MANE Select ENSP00000420840.3:p.Ala363Asp
ENST00000378133.4:c.1088C>A ENSP00000367373.3:p.Ala363Asp
ENST00000394633.7:c.1088C>A ENSP00000378129.3:p.Ala363Asp
ENST00000504120.3:c.1088C>A ENSP00000420840.2:p.Ala363Asp
NM_018900.3:c.1088C>A NP_061723.1:p.Ala363Asp
NM_031410.2:c.1088C>A NP_113598.1:p.Ala363Asp
NM_031411.2:c.1088C>A NP_113599.1:p.Ala363Asp
NM_018900.4:c.1088C>A MANE Select NP_061723.1:p.Ala363Asp
NM_031411.3:c.1088C>A NP_113599.1:p.Ala363Asp
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Search 100 bp 3'