Canonical Allele Identifier: CA2030189160
Gene: CPNE8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.38656818C= , CM000674.2:g.38656818C= GRCh38
NC_000012.11:g.39050620C= , CM000674.1:g.39050620C= GRCh37
NC_000012.10:g.37336887C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000331366.10:c.1507-2748G= MANE Select ENSP00000329748.5:n.1507-2748G=
ENST00000331366.9:c.1507-2748G= ENSP00000329748.5:n.1507-2748G=
ENST00000360449.3:c.1471-2748G= ENSP00000353633.3:n.1471-2748G=
ENST00000538596.6:c.514-2748G= ENSP00000439237.2:n.514-2748G=
ENST00000546603.5:n.337-2748G=
ENST00000547417.1:n.268-2748G=
ENST00000552259.5:n.281-9725G=
NM_153634.2:c.1507-2748G= NP_705898.1:n.1507-2748G=
XR_944501.1:n.2219-2748G=
XM_017018852.1:c.1024-2748G= XP_016874341.1:n.1024-2748G=
XR_944501.3:n.1675-2748G=
NM_153634.3:c.1507-2748G= MANE Select NP_705898.1:n.1507-2748G=
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