Canonical Allele Identifier: CA2661497322

Gene: CACNB4

Linked Data

• gnomAD v4: 2-152098869-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.152098869A>G , CM000664.2:g.152098869A>G	GRCh38
NC_000002.11:g.152955383A>G , CM000664.1:g.152955383A>G	GRCh37
NC_000002.10:g.152663629A>G	NCBI36
NG_012641.1:g.5211T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000201943.10:c.63+80T>C	ENSP00000201943.5:n.63+80T>C
ENST00000427385.6:c.63+80T>C	ENSP00000410978.2:n.63+80T>C
ENST00000470066.2:n.192+80T>C
ENST00000539935.7:c.63+80T>C MANE Select	ENSP00000438949.1:n.63+80T>C
ENST00000637309.1:c.63+80T>C	ENSP00000490127.1:n.63+80T>C
ENST00000201943.9:c.63+80T>C	ENSP00000201943.5:n.63+80T>C
ENST00000539935.5:c.63+80T>C	ENSP00000438949.1:n.63+80T>C
NM_000726.3:c.63+80T>C	NP_000717.2:n.63+80T>C
NM_001145798.1:c.63+80T>C	NP_001139270.1:n.63+80T>C
XM_011511797.1:c.63+80T>C	XP_011510099.1:n.63+80T>C
XM_011511798.1:c.63+80T>C	XP_011510100.1:n.63+80T>C
XM_011511799.1:c.63+80T>C	XP_011510101.1:n.63+80T>C
XR_923022.1:n.1040+80T>C
XR_923023.1:n.1040+80T>C
NM_000726.4:c.63+80T>C	NP_000717.2:n.63+80T>C
NM_001005746.3:c.-220T>C	NP_001005746.1:n.-220T>C
NM_001145798.2:c.63+80T>C	NP_001139270.1:n.63+80T>C
NM_001330113.1:c.-220T>C	NP_001317042.1:n.-220T>C
XM_011511797.3:c.63+80T>C	XP_011510099.1:n.63+80T>C
XR_002959337.1:n.216+80T>C
XR_923022.3:n.216+80T>C
NM_000726.5:c.63+80T>C MANE Select	NP_000717.2:n.63+80T>C