Canonical Allele Identifier: CA2030189042
Gene: CPNE8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.38656713A= , CM000674.2:g.38656713A= GRCh38
NC_000012.11:g.39050515A= , CM000674.1:g.39050515A= GRCh37
NC_000012.10:g.37336782A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000331366.10:c.1507-2643T= MANE Select ENSP00000329748.5:n.1507-2643T=
ENST00000331366.9:c.1507-2643T= ENSP00000329748.5:n.1507-2643T=
ENST00000360449.3:c.1471-2643T= ENSP00000353633.3:n.1471-2643T=
ENST00000538596.6:c.514-2643T= ENSP00000439237.2:n.514-2643T=
ENST00000546603.5:n.337-2643T=
ENST00000547417.1:n.268-2643T=
ENST00000552259.5:n.281-9620T=
NM_153634.2:c.1507-2643T= NP_705898.1:n.1507-2643T=
XR_944501.1:n.2219-2643T=
XM_017018852.1:c.1024-2643T= XP_016874341.1:n.1024-2643T=
XR_944501.3:n.1675-2643T=
NM_153634.3:c.1507-2643T= MANE Select NP_705898.1:n.1507-2643T=
Search 100 bp 5'
Search 100 bp 3'