Canonical Allele Identifier: CA1931597277
Gene: CPN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100045624G= , CM000672.2:g.100045624G= GRCh38
NC_000010.10:g.101805381G= , CM000672.1:g.101805381G= GRCh37
NC_000010.9:g.101795371G= NCBI36
NG_012060.1:g.41262C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370418.8:c.1231-3051C= MANE Select ENSP00000359446.3:n.1231-3051C=
ENST00000370418.7:c.1231-3051C= ENSP00000359446.3:n.1231-3051C=
NM_001308.2:c.1231-3051C= NP_001299.1:n.1231-3051C=
XM_011539299.1:c.1273-3051C= XP_011537601.1:n.1273-3051C=
NM_001308.3:c.1231-3051C= MANE Select NP_001299.1:n.1231-3051C=