Canonical Allele Identifier: CA2030189056

Gene: CPNE8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.38656727T= , CM000674.2:g.38656727T=	GRCh38
NC_000012.11:g.39050529T= , CM000674.1:g.39050529T=	GRCh37
NC_000012.10:g.37336796T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331366.10:c.1507-2657A= MANE Select	ENSP00000329748.5:n.1507-2657A=
ENST00000331366.9:c.1507-2657A=	ENSP00000329748.5:n.1507-2657A=
ENST00000360449.3:c.1471-2657A=	ENSP00000353633.3:n.1471-2657A=
ENST00000538596.6:c.514-2657A=	ENSP00000439237.2:n.514-2657A=
ENST00000546603.5:n.337-2657A=
ENST00000547417.1:n.268-2657A=
ENST00000552259.5:n.281-9634A=
NM_153634.2:c.1507-2657A=	NP_705898.1:n.1507-2657A=
XR_944501.1:n.2219-2657A=
XM_017018852.1:c.1024-2657A=	XP_016874341.1:n.1024-2657A=
XR_944501.3:n.1675-2657A=
NM_153634.3:c.1507-2657A= MANE Select	NP_705898.1:n.1507-2657A=