Canonical Allele Identifier: CA1360257906

Gene: CCK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42258378C= , CM000665.2:g.42258378C=	GRCh38
NC_000003.11:g.42299870C= , CM000665.1:g.42299870C=	GRCh37
NC_000003.10:g.42274874C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396169.7:c.215-147G= MANE Select	ENSP00000379472.2:n.215-147G=
ENST00000334681.9:c.215-147G=	ENSP00000335657.5:n.215-147G=
ENST00000396169.6:c.215-147G=	ENSP00000379472.2:n.215-147G=
ENST00000434608.1:c.215-147G=	ENSP00000409124.1:n.215-147G=
NM_000729.4:c.215-147G=	NP_000720.1:n.215-147G=
NM_001174138.1:c.215-147G=	NP_001167609.1:n.215-147G=
NM_000729.5:c.215-147G=	NP_000720.1:n.215-147G=
NM_001174138.2:c.215-147G=	NP_001167609.1:n.215-147G=
NM_000729.6:c.215-147G= MANE Select	NP_000720.1:n.215-147G=
NM_001174138.3:c.215-147G=	NP_001167609.1:n.215-147G=