Canonical Allele Identifier: CA658846462

Gene: CPN1

Linked Data

• dbSNP Id: rs1457067818
• MyVariant Identifiers: chr10:g.101805359A>G (hg19) ; chr10:g.100045602A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100045602A>G , CM000672.2:g.100045602A>G	GRCh38
NC_000010.10:g.101805359A>G , CM000672.1:g.101805359A>G	GRCh37
NC_000010.9:g.101795349A>G	NCBI36
NG_012060.1:g.41284T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370418.8:c.1231-3029T>C MANE Select	ENSP00000359446.3:n.1231-3029T>C
ENST00000370418.7:c.1231-3029T>C	ENSP00000359446.3:n.1231-3029T>C
NM_001308.2:c.1231-3029T>C	NP_001299.1:n.1231-3029T>C
XM_011539299.1:c.1273-3029T>C	XP_011537601.1:n.1273-3029T>C
NM_001308.3:c.1231-3029T>C MANE Select	NP_001299.1:n.1231-3029T>C