Canonical Allele Identifier: CA658846473
Gene: CPN1 HGNC NCBI

Linked Data

dbSNP Id: rs1387030139
MyVariant Identifiers: chr10:g.101805396T>G (hg19) chr10:g.100045639T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100045639T>G , CM000672.2:g.100045639T>G GRCh38
NC_000010.10:g.101805396T>G , CM000672.1:g.101805396T>G GRCh37
NC_000010.9:g.101795386T>G NCBI36
NG_012060.1:g.41247A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370418.8:c.1231-3066A>C MANE Select ENSP00000359446.3:n.1231-3066A>C
ENST00000370418.7:c.1231-3066A>C ENSP00000359446.3:n.1231-3066A>C
NM_001308.2:c.1231-3066A>C NP_001299.1:n.1231-3066A>C
XM_011539299.1:c.1273-3066A>C XP_011537601.1:n.1273-3066A>C
NM_001308.3:c.1231-3066A>C MANE Select NP_001299.1:n.1231-3066A>C
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