Canonical Allele Identifier: CA1754647987
Gene: CNPY1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155492416A= , CM000669.2:g.155492416A= GRCh38
NC_000007.13:g.155285111A= , CM000669.1:g.155285111A= GRCh37
NC_000007.12:g.154977872A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000635903.1:n.1217-8531T=
ENST00000406197.5:c.*47+10605T= ENSP00000384514.1:n.*47+10605T=