Canonical Allele Identifier: CA1572802619
Gene: CAMK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111436706C= , CM000667.2:g.111436706C= GRCh38
NC_000005.9:g.110772404C= , CM000667.1:g.110772404C= GRCh37
NC_000005.8:g.110800303C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000282356.9:c.460-9980C= MANE Select ENSP00000282356.4:n.460-9980C=
ENST00000282356.8:c.460-9980C= ENSP00000282356.4:n.460-9980C=
ENST00000502916.5:n.384-9980C=
ENST00000504544.5:c.*47-9980C= ENSP00000423761.1:n.*47-9980C=
ENST00000505763.1:n.360-9980C=
ENST00000512453.5:c.460-9980C= ENSP00000422634.1:n.460-9980C=
ENST00000514007.5:c.*47-9980C= ENSP00000421606.1:n.*47-9980C=
ENST00000515231.5:c.*47-9980C= ENSP00000424912.1:n.*47-9980C=
NM_001744.4:c.460-9980C= NP_001735.1:n.460-9980C=
XR_948301.1:n.518-9980C=
XR_948302.1:n.518-9980C=
XR_948303.1:n.518-9980C=
NM_001323374.1:c.460-9980C= NP_001310303.1:n.460-9980C=
NM_001323375.1:c.460-9980C= NP_001310304.1:n.460-9980C=
NM_001323376.1:c.-132-9980C= NP_001310305.1:n.-132-9980C=
NM_001323377.1:c.-132-9980C= NP_001310306.1:n.-132-9980C=
NM_001744.5:c.460-9980C= NP_001735.1:n.460-9980C=
XR_001742281.2:n.560-9980C=
XR_001742282.2:n.560-9980C=
XR_948303.2:n.560-9980C=
NM_001744.6:c.460-9980C= MANE Select NP_001735.1:n.460-9980C=
NM_001323374.2:c.460-9980C= NP_001310303.1:n.460-9980C=
NM_001323375.2:c.460-9980C= NP_001310304.1:n.460-9980C=
NM_001323376.2:c.-132-9980C= NP_001310305.1:n.-132-9980C=
NM_001323377.2:c.-132-9980C= NP_001310306.1:n.-132-9980C=