Canonical Allele Identifier: CA1931597255
Gene: CPN1 HGNC NCBI

Linked Data

dbSNP Id: rs1564769761

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100045582T>C , CM000672.2:g.100045582T>C GRCh38
NC_000010.10:g.101805339T>C , CM000672.1:g.101805339T>C GRCh37
NC_000010.9:g.101795329T>C NCBI36
NG_012060.1:g.41304A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370418.8:c.1231-3009A>G MANE Select ENSP00000359446.3:n.1231-3009A>G
ENST00000370418.7:c.1231-3009A>G ENSP00000359446.3:n.1231-3009A>G
NM_001308.2:c.1231-3009A>G NP_001299.1:n.1231-3009A>G
XM_011539299.1:c.1273-3009A>G XP_011537601.1:n.1273-3009A>G
NM_001308.3:c.1231-3009A>G MANE Select NP_001299.1:n.1231-3009A>G