Canonical Allele Identifier: CA658846492

Gene: CPN1

Linked Data

• dbSNP Id: rs1275076346
• gnomAD v3: 10-100045734-G-C
• gnomAD v4: 10-100045734-G-C
• MyVariant Identifiers: chr10:g.101805491G>C (hg19) ; chr10:g.100045734G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100045734G>C , CM000672.2:g.100045734G>C	GRCh38
NC_000010.10:g.101805491G>C , CM000672.1:g.101805491G>C	GRCh37
NC_000010.9:g.101795481G>C	NCBI36
NG_012060.1:g.41152C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370418.8:c.1230+3024C>G MANE Select	ENSP00000359446.3:n.1230+3024C>G
ENST00000370418.7:c.1230+3024C>G	ENSP00000359446.3:n.1230+3024C>G
NM_001308.2:c.1230+3024C>G	NP_001299.1:n.1230+3024C>G
XM_011539299.1:c.1272+3024C>G	XP_011537601.1:n.1272+3024C>G
NM_001308.3:c.1230+3024C>G MANE Select	NP_001299.1:n.1230+3024C>G