Canonical Allele Identifier: CA1365813944

Gene: CACNA2D3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.54496558G>T , CM000665.2:g.54496558G>T	GRCh38
NC_000003.11:g.54530585G>T , CM000665.1:g.54530585G>T	GRCh37
NC_000003.10:g.54505625G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474759.6:c.382-6934G>T MANE Select	ENSP00000419101.1:n.382-6934G>T
ENST00000288197.9:c.382-6934G>T	ENSP00000288197.5:n.382-6934G>T
ENST00000415676.6:c.382-6934G>T	ENSP00000389506.2:n.382-6934G>T
ENST00000468658.1:c.100-66242G>T	ENSP00000417455.1:n.100-66242G>T
ENST00000471363.5:c.100-6934G>T	ENSP00000418228.1:n.100-6934G>T
ENST00000474759.5:c.382-6934G>T	ENSP00000419101.1:n.382-6934G>T
ENST00000477024.5:c.100-6934G>T	ENSP00000417318.1:n.100-6934G>T
ENST00000490478.5:c.100-6934G>T	ENSP00000417279.1:n.100-6934G>T
ENST00000492460.5:c.100-6934G>T	ENSP00000418028.1:n.100-6934G>T
ENST00000620722.4:c.100-6934G>T	ENSP00000478969.1:n.100-6934G>T
NM_018398.2:c.382-6934G>T	NP_060868.2:n.382-6934G>T
XM_005265318.1:c.382-6934G>T	XP_005265375.1:n.382-6934G>T
XM_011533946.1:c.382-6934G>T	XP_011532248.1:n.382-6934G>T
XM_011533947.1:c.382-6934G>T	XP_011532249.1:n.382-6934G>T
XM_011533948.1:c.382-6934G>T	XP_011532250.1:n.382-6934G>T
XM_011533949.1:c.382-6934G>T	XP_011532251.1:n.382-6934G>T
XM_011533950.1:c.382-6934G>T	XP_011532252.1:n.382-6934G>T
XM_011533951.1:c.382-6934G>T	XP_011532253.1:n.382-6934G>T
XM_011533952.1:c.382-6934G>T	XP_011532254.1:n.382-6934G>T
XM_011533953.1:c.382-6934G>T	XP_011532255.1:n.382-6934G>T
XR_427281.1:n.503-6934G>T
XR_427282.2:n.503-6934G>T
XR_940472.1:n.503-6934G>T
XR_940473.1:n.503-6934G>T
XM_005265318.2:c.382-6934G>T	XP_005265375.1:n.382-6934G>T
XM_011533946.2:c.382-6934G>T	XP_011532248.1:n.382-6934G>T
XM_011533947.2:c.382-6934G>T	XP_011532249.1:n.382-6934G>T
XM_011533949.2:c.382-6934G>T	XP_011532251.1:n.382-6934G>T
XM_011533950.2:c.382-6934G>T	XP_011532252.1:n.382-6934G>T
XM_011533951.2:c.382-6934G>T	XP_011532253.1:n.382-6934G>T
XM_011533952.2:c.382-6934G>T	XP_011532254.1:n.382-6934G>T
XM_011533953.2:c.382-6934G>T	XP_011532255.1:n.382-6934G>T
XM_017006850.1:c.382-6934G>T	XP_016862339.1:n.382-6934G>T
XM_017006851.2:c.-150-6934G>T	XP_016862340.1:n.-150-6934G>T
XM_017006852.1:c.382-6934G>T	XP_016862341.1:n.382-6934G>T
XM_024453640.1:c.100-6934G>T	XP_024309408.1:n.100-6934G>T
XR_001740203.1:n.502-6934G>T
XR_001740204.1:n.502-6934G>T
XR_001740205.1:n.502-6934G>T
XR_002959549.1:n.502-6934G>T
XR_427281.2:n.502-6934G>T
XR_940472.2:n.502-6934G>T
XR_940473.2:n.502-6934G>T
NM_018398.3:c.382-6934G>T MANE Select	NP_060868.2:n.382-6934G>T