Canonical Allele Identifier: CA1891244262

Gene: CAMK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.12660716G= , CM000672.2:g.12660716G=	GRCh38
NC_000010.10:g.12702715G= , CM000672.1:g.12702715G=	GRCh37
NC_000010.9:g.12742721G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619168.5:c.225-6020G= MANE Select	ENSP00000478874.1:n.225-6020G=
ENST00000378845.5:c.225-6020G=	ENSP00000368122.1:n.225-6020G=
ENST00000487696.1:n.260-6020G=
ENST00000619168.4:c.225-6020G=	ENSP00000478874.1:n.225-6020G=
NM_020397.3:c.225-6020G=	NP_065130.1:n.225-6020G=
NM_153498.3:c.225-6020G=	NP_705718.1:n.225-6020G=
XM_006717481.2:c.168-6020G=	XP_006717544.1:n.168-6020G=
XM_006717482.2:c.225-6020G=	XP_006717545.1:n.225-6020G=
XM_006717483.2:c.225-6020G=	XP_006717546.1:n.225-6020G=
XM_011519591.1:c.186-6020G=	XP_011517893.1:n.186-6020G=
XM_011519595.1:c.-67-6020G=	XP_011517897.1:n.-67-6020G=
NM_001351032.1:c.-67-6020G=	NP_001337961.1:n.-67-6020G=
XM_006717482.3:c.225-6020G=	XP_006717545.1:n.225-6020G=
XM_006717483.4:c.225-6020G=	XP_006717546.1:n.225-6020G=
XM_011519591.3:c.186-6020G=	XP_011517893.1:n.186-6020G=
XM_011519595.3:c.-67-6020G=	XP_011517897.1:n.-67-6020G=
XM_017016438.2:c.-67-6020G=	XP_016871927.1:n.-67-6020G=
XM_024448087.1:c.-67-6020G=	XP_024303855.1:n.-67-6020G=
NM_001351032.2:c.-67-6020G=	NP_001337961.1:n.-67-6020G=
NM_020397.4:c.225-6020G=	NP_065130.1:n.225-6020G=
NM_153498.4:c.225-6020G= MANE Select	NP_705718.1:n.225-6020G=