Canonical Allele Identifier: CA212878496
Gene: CPN1 HGNC NCBI

Linked Data

dbSNP Id: rs985346287
gnomAD v2: 10-101805411-C-T
gnomAD v3: 10-100045654-C-T
gnomAD v4: 10-100045654-C-T
MyVariant Identifiers: chr10:g.101805411C>T (hg19) chr10:g.100045654C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100045654C>T , CM000672.2:g.100045654C>T GRCh38
NC_000010.10:g.101805411C>T , CM000672.1:g.101805411C>T GRCh37
NC_000010.9:g.101795401C>T NCBI36
NG_012060.1:g.41232G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370418.8:c.1231-3081G>A MANE Select ENSP00000359446.3:n.1231-3081G>A
ENST00000370418.7:c.1231-3081G>A ENSP00000359446.3:n.1231-3081G>A
NM_001308.2:c.1231-3081G>A NP_001299.1:n.1231-3081G>A
XM_011539299.1:c.1273-3081G>A XP_011537601.1:n.1273-3081G>A
NM_001308.3:c.1231-3081G>A MANE Select NP_001299.1:n.1231-3081G>A
Search 100 bp 5'
Search 100 bp 3'