Canonical Allele Identifier: CA2030189134

Gene: CPNE8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.38656799A= , CM000674.2:g.38656799A=	GRCh38
NC_000012.11:g.39050601A= , CM000674.1:g.39050601A=	GRCh37
NC_000012.10:g.37336868A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331366.10:c.1507-2729T= MANE Select	ENSP00000329748.5:n.1507-2729T=
ENST00000331366.9:c.1507-2729T=	ENSP00000329748.5:n.1507-2729T=
ENST00000360449.3:c.1471-2729T=	ENSP00000353633.3:n.1471-2729T=
ENST00000538596.6:c.514-2729T=	ENSP00000439237.2:n.514-2729T=
ENST00000546603.5:n.337-2729T=
ENST00000547417.1:n.268-2729T=
ENST00000552259.5:n.281-9706T=
NM_153634.2:c.1507-2729T=	NP_705898.1:n.1507-2729T=
XR_944501.1:n.2219-2729T=
XM_017018852.1:c.1024-2729T=	XP_016874341.1:n.1024-2729T=
XR_944501.3:n.1675-2729T=
NM_153634.3:c.1507-2729T= MANE Select	NP_705898.1:n.1507-2729T=