Canonical Allele Identifier: CA688609330

Gene: CPNE8

Linked Data

• dbSNP Id: rs1298926735
• gnomAD v3: 12-38656836-A-T
• gnomAD v4: 12-38656836-A-T
• MyVariant Identifiers: chr12:g.39050638A>T (hg19) ; chr12:g.38656836A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.38656836A>T , CM000674.2:g.38656836A>T	GRCh38
NC_000012.11:g.39050638A>T , CM000674.1:g.39050638A>T	GRCh37
NC_000012.10:g.37336905A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331366.10:c.1507-2766T>A MANE Select	ENSP00000329748.5:n.1507-2766T>A
ENST00000331366.9:c.1507-2766T>A	ENSP00000329748.5:n.1507-2766T>A
ENST00000360449.3:c.1471-2766T>A	ENSP00000353633.3:n.1471-2766T>A
ENST00000538596.6:c.514-2766T>A	ENSP00000439237.2:n.514-2766T>A
ENST00000546603.5:n.337-2766T>A
ENST00000547417.1:n.268-2766T>A
ENST00000552259.5:n.281-9743T>A
NM_153634.2:c.1507-2766T>A	NP_705898.1:n.1507-2766T>A
XR_944501.1:n.2219-2766T>A
XM_017018852.1:c.1024-2766T>A	XP_016874341.1:n.1024-2766T>A
XR_944501.3:n.1675-2766T>A
NM_153634.3:c.1507-2766T>A MANE Select	NP_705898.1:n.1507-2766T>A