Canonical Allele Identifier: CA447045399
Gene: PCDHGA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.140710605T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141331038T>C , CM000667.2:g.141331038T>C GRCh38
NC_000005.9:g.140710605T>C , CM000667.1:g.140710605T>C GRCh37
NC_000005.8:g.140690789T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000517417.3:c.354T>C MANE Select ENSP00000431083.1:p.Pro118=
ENST00000378105.4:c.354T>C ENSP00000367345.3:p.Pro118=
ENST00000517417.2:c.354T>C ENSP00000431083.1:p.Pro118=
NM_018912.2:c.354T>C NP_061735.1:p.Pro118=
NM_031993.1:c.354T>C NP_114382.1:p.Pro118=
NM_018912.3:c.354T>C MANE Select NP_061735.1:p.Pro118=
NM_031993.2:c.354T>C NP_114382.1:p.Pro118=