Canonical Allele Identifier: CA1931597314
Gene: CPN1 HGNC NCBI

Linked Data

dbSNP Id: rs2041303761
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100045696T>A , CM000672.2:g.100045696T>A GRCh38
NC_000010.10:g.101805453T>A , CM000672.1:g.101805453T>A GRCh37
NC_000010.9:g.101795443T>A NCBI36
NG_012060.1:g.41190A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370418.8:c.1230+3062A>T MANE Select ENSP00000359446.3:n.1230+3062A>T
ENST00000370418.7:c.1230+3062A>T ENSP00000359446.3:n.1230+3062A>T
NM_001308.2:c.1230+3062A>T NP_001299.1:n.1230+3062A>T
XM_011539299.1:c.1272+3062A>T XP_011537601.1:n.1272+3062A>T
NM_001308.3:c.1230+3062A>T MANE Select NP_001299.1:n.1230+3062A>T
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