Canonical Allele Identifier: CA1298490881
Gene: CACNB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.152098871G= , CM000664.2:g.152098871G= GRCh38
NC_000002.11:g.152955385G= , CM000664.1:g.152955385G= GRCh37
NC_000002.10:g.152663631G= NCBI36
NG_012641.1:g.5209C=

Transcript Alleles

HGVS Amino-acid change
ENST00000201943.10:c.63+78C= ENSP00000201943.5:n.63+78C=
ENST00000427385.6:c.63+78C= ENSP00000410978.2:n.63+78C=
ENST00000470066.2:n.192+78C=
ENST00000539935.7:c.63+78C= MANE Select ENSP00000438949.1:n.63+78C=
ENST00000637309.1:c.63+78C= ENSP00000490127.1:n.63+78C=
ENST00000201943.9:c.63+78C= ENSP00000201943.5:n.63+78C=
ENST00000539935.5:c.63+78C= ENSP00000438949.1:n.63+78C=
NM_000726.3:c.63+78C= NP_000717.2:n.63+78C=
NM_001145798.1:c.63+78C= NP_001139270.1:n.63+78C=
XM_011511797.1:c.63+78C= XP_011510099.1:n.63+78C=
XM_011511798.1:c.63+78C= XP_011510100.1:n.63+78C=
XM_011511799.1:c.63+78C= XP_011510101.1:n.63+78C=
XR_923022.1:n.1040+78C=
XR_923023.1:n.1040+78C=
NM_000726.4:c.63+78C= NP_000717.2:n.63+78C=
NM_001005746.3:c.-222C= NP_001005746.1:n.-222C=
NM_001145798.2:c.63+78C= NP_001139270.1:n.63+78C=
NM_001330113.1:c.-222C= NP_001317042.1:n.-222C=
XM_011511797.3:c.63+78C= XP_011510099.1:n.63+78C=
XR_002959337.1:n.216+78C=
XR_923022.3:n.216+78C=
NM_000726.5:c.63+78C= MANE Select NP_000717.2:n.63+78C=