Canonical Allele Identifier: CA1363936549

Gene: CACNA2D2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50402995A= , CM000665.2:g.50402995A=	GRCh38
NC_000003.11:g.50440426A= , CM000665.1:g.50440426A=	GRCh37
NC_000003.10:g.50415430A=	NCBI36
NG_034070.1:g.106250T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424201.7:c.406-8827T= MANE Select	ENSP00000390329.2:n.406-8827T=
ENST00000266039.7:c.406-8827T=	ENSP00000266039.3:n.406-8827T=
ENST00000360963.7:c.199-8827T=	ENSP00000354228.3:n.199-8827T=
ENST00000423994.6:c.406-8827T=	ENSP00000407393.2:n.406-8827T=
ENST00000424201.6:c.406-8827T=	ENSP00000390329.2:n.406-8827T=
ENST00000429770.5:c.406-8827T=	ENSP00000404631.1:n.406-8827T=
ENST00000479441.1:c.406-8827T=	ENSP00000418081.1:n.406-8827T=
NM_001005505.2:c.406-8827T=	NP_001005505.1:n.406-8827T=
NM_001174051.2:c.406-8827T=	NP_001167522.1:n.406-8827T=
NM_001291101.1:c.199-8827T=	NP_001278030.1:n.199-8827T=
NM_006030.3:c.406-8827T=	NP_006021.2:n.406-8827T=
XM_005265581.3:c.406-8827T=	XP_005265638.1:n.406-8827T=
XM_011534242.1:c.406-8827T=	XP_011532544.1:n.406-8827T=
XM_011534243.1:c.406-8827T=	XP_011532545.1:n.406-8827T=
XM_011534244.1:c.406-8827T=	XP_011532546.1:n.406-8827T=
XM_005265581.4:c.406-8827T=	XP_005265638.1:n.406-8827T=
XM_011534243.2:c.406-8827T=	XP_011532545.1:n.406-8827T=
NM_001005505.3:c.406-8827T=	NP_001005505.1:n.406-8827T=
NM_001174051.3:c.406-8827T=	NP_001167522.1:n.406-8827T=
NM_006030.4:c.406-8827T= MANE Select	NP_006021.2:n.406-8827T=