Canonical Allele Identifier: CA1754647931
Gene: CNPY1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155492340C= , CM000669.2:g.155492340C= GRCh38
NC_000007.13:g.155285035C= , CM000669.1:g.155285035C= GRCh37
NC_000007.12:g.154977796C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000635903.1:n.1217-8455G=
ENST00000406197.5:c.*47+10681G= ENSP00000384514.1:n.*47+10681G=