Canonical Allele Identifier: CA361339258
Gene: PCDHGA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.140710617A>C (hg19) chr5:g.141331050A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141331050A>C , CM000667.2:g.141331050A>C GRCh38
NC_000005.9:g.140710617A>C , CM000667.1:g.140710617A>C GRCh37
NC_000005.8:g.140690801A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000517417.3:c.366A>C MANE Select ENSP00000431083.1:p.Glu122Asp
ENST00000378105.4:c.366A>C ENSP00000367345.3:p.Glu122Asp
ENST00000517417.2:c.366A>C ENSP00000431083.1:p.Glu122Asp
NM_018912.2:c.366A>C NP_061735.1:p.Glu122Asp
NM_031993.1:c.366A>C NP_114382.1:p.Glu122Asp
NM_018912.3:c.366A>C MANE Select NP_061735.1:p.Glu122Asp
NM_031993.2:c.366A>C NP_114382.1:p.Glu122Asp
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