Canonical Allele Identifier: CA13273705
Gene: CPN1 HGNC NCBI

Linked Data

dbSNP Id: rs4462272

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100063786T>C , CM000672.2:g.100063786T>C GRCh38
NC_000010.10:g.101823543T>C , CM000672.1:g.101823543T>C GRCh37
NC_000010.9:g.101813533T>C NCBI36
NG_012060.1:g.23100A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370418.8:c.760-61A>G MANE Select ENSP00000359446.3:n.760-61A>G
ENST00000370418.7:c.760-61A>G ENSP00000359446.3:n.760-61A>G
ENST00000441382.1:c.151-61A>G ENSP00000410895.1:n.151-61A>G
NM_001308.2:c.760-61A>G NP_001299.1:n.760-61A>G
XM_011539299.1:c.802-61A>G XP_011537601.1:n.802-61A>G
NM_001308.3:c.760-61A>G MANE Select NP_001299.1:n.760-61A>G