Canonical Allele Identifier: CA1891232272
Gene: CAMK1D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.12633071G= , CM000672.2:g.12633071G= GRCh38
NC_000010.10:g.12675070G= , CM000672.1:g.12675070G= GRCh37
NC_000010.9:g.12715076G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000619168.5:c.225-33665G= MANE Select ENSP00000478874.1:n.225-33665G=
ENST00000378845.5:c.225-33665G= ENSP00000368122.1:n.225-33665G=
ENST00000487696.1:n.260-33665G=
ENST00000619168.4:c.225-33665G= ENSP00000478874.1:n.225-33665G=
NM_020397.3:c.225-33665G= NP_065130.1:n.225-33665G=
NM_153498.3:c.225-33665G= NP_705718.1:n.225-33665G=
XM_006717481.2:c.168-33665G= XP_006717544.1:n.168-33665G=
XM_006717482.2:c.225-33665G= XP_006717545.1:n.225-33665G=
XM_006717483.2:c.225-33665G= XP_006717546.1:n.225-33665G=
XM_011519591.1:c.186-33665G= XP_011517893.1:n.186-33665G=
NM_001351032.1:c.-67-33665G= NP_001337961.1:n.-67-33665G=
XM_006717482.3:c.225-33665G= XP_006717545.1:n.225-33665G=
XM_006717483.4:c.225-33665G= XP_006717546.1:n.225-33665G=
XM_011519591.3:c.186-33665G= XP_011517893.1:n.186-33665G=
XM_017016438.2:c.-67-33665G= XP_016871927.1:n.-67-33665G=
XM_024448087.1:c.-67-33665G= XP_024303855.1:n.-67-33665G=
NM_001351032.2:c.-67-33665G= NP_001337961.1:n.-67-33665G=
NM_020397.4:c.225-33665G= NP_065130.1:n.225-33665G=
NM_153498.4:c.225-33665G= MANE Select NP_705718.1:n.225-33665G=