Canonical Allele Identifier: CA1891194920
Gene: CAMK1D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.12549726T= , CM000672.2:g.12549726T= GRCh38
NC_000010.10:g.12591725T= , CM000672.1:g.12591725T= GRCh37
NC_000010.9:g.12631731T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000619168.5:c.93-3499T= MANE Select ENSP00000478874.1:n.93-3499T=
ENST00000378845.5:c.93-3499T= ENSP00000368122.1:n.93-3499T=
ENST00000487696.1:n.260-117010T=
ENST00000619168.4:c.93-3499T= ENSP00000478874.1:n.93-3499T=
NM_020397.3:c.93-3499T= NP_065130.1:n.93-3499T=
NM_153498.3:c.93-3499T= NP_705718.1:n.93-3499T=
XM_006717481.2:c.36-3499T= XP_006717544.1:n.36-3499T=
XM_006717482.2:c.93-3499T= XP_006717545.1:n.93-3499T=
XM_006717483.2:c.93-3499T= XP_006717546.1:n.93-3499T=
XM_011519591.1:c.54-3499T= XP_011517893.1:n.54-3499T=
NM_001351032.1:c.-199-3499T= NP_001337961.1:n.-199-3499T=
XM_006717482.3:c.93-3499T= XP_006717545.1:n.93-3499T=
XM_006717483.4:c.93-3499T= XP_006717546.1:n.93-3499T=
XM_011519591.3:c.54-3499T= XP_011517893.1:n.54-3499T=
XM_017016438.2:c.-199-3499T= XP_016871927.1:n.-199-3499T=
XM_024448087.1:c.-199-3499T= XP_024303855.1:n.-199-3499T=
NM_001351032.2:c.-199-3499T= NP_001337961.1:n.-199-3499T=
NM_020397.4:c.93-3499T= NP_065130.1:n.93-3499T=
NM_153498.4:c.93-3499T= MANE Select NP_705718.1:n.93-3499T=