Canonical Allele Identifier: CA595465149
Gene: CPN1 HGNC NCBI

Linked Data

dbSNP Id: rs1250467767
gnomAD v2: 10-101805438-G-GT
gnomAD v3: 10-100045681-G-GT
gnomAD v4: 10-100045681-G-GT
MyVariant Identifiers: chr10:g.101805438_101805439insT (hg19) chr10:g.100045681_100045682insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100045684dup , CM000672.2:g.100045684dup GRCh38
NC_000010.10:g.101805441dup , CM000672.1:g.101805441dup GRCh37
NC_000010.9:g.101795431dup NCBI36
NG_012060.1:g.41204dup

Transcript Alleles

HGVS Amino-acid change
ENST00000370418.8:c.1230+3076dup MANE Select ENSP00000359446.3:n.1230+3076dup
ENST00000370418.7:c.1230+3076dup ENSP00000359446.3:n.1230+3076dup
NM_001308.2:c.1230+3076dup NP_001299.1:n.1230+3076dup
XM_011539299.1:c.1272+3076dup XP_011537601.1:n.1272+3076dup
NM_001308.3:c.1230+3076dup MANE Select NP_001299.1:n.1230+3076dup
Search 100 bp 5'
Search 100 bp 3'