Canonical Allele Identifier: CA1931597239
Gene: CPN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100045564A= , CM000672.2:g.100045564A= GRCh38
NC_000010.10:g.101805321A= , CM000672.1:g.101805321A= GRCh37
NC_000010.9:g.101795311A= NCBI36
NG_012060.1:g.41322T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370418.8:c.1231-2991T= MANE Select ENSP00000359446.3:n.1231-2991T=
ENST00000370418.7:c.1231-2991T= ENSP00000359446.3:n.1231-2991T=
NM_001308.2:c.1231-2991T= NP_001299.1:n.1231-2991T=
XM_011539299.1:c.1273-2991T= XP_011537601.1:n.1273-2991T=
NM_001308.3:c.1231-2991T= MANE Select NP_001299.1:n.1231-2991T=
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