Canonical Allele Identifier: CA1891085364

Gene: CAMK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.12396784G= , CM000672.2:g.12396784G=	GRCh38
NC_000010.10:g.12438783G= , CM000672.1:g.12438783G=	GRCh37
NC_000010.9:g.12478789G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619168.5:c.92+46874G= MANE Select	ENSP00000478874.1:n.92+46874G=
ENST00000378845.5:c.92+46874G=	ENSP00000368122.1:n.92+46874G=
ENST00000487696.1:n.259+46874G=
ENST00000619168.4:c.92+46874G=	ENSP00000478874.1:n.92+46874G=
NM_020397.3:c.92+46874G=	NP_065130.1:n.92+46874G=
NM_153498.3:c.92+46874G=	NP_705718.1:n.92+46874G=
XM_006717482.2:c.92+46874G=	XP_006717545.1:n.92+46874G=
XM_006717483.2:c.92+46874G=	XP_006717546.1:n.92+46874G=
XM_011519591.1:c.53+7727G=	XP_011517893.1:n.53+7727G=
NM_001351032.1:c.-467-6318G=	NP_001337961.1:n.-467-6318G=
XM_006717482.3:c.92+46874G=	XP_006717545.1:n.92+46874G=
XM_006717483.4:c.92+46874G=	XP_006717546.1:n.92+46874G=
XM_011519591.3:c.53+7727G=	XP_011517893.1:n.53+7727G=
XM_017016438.2:c.-467-6318G=	XP_016871927.1:n.-467-6318G=
XM_024448087.1:c.-467-6318G=	XP_024303855.1:n.-467-6318G=
NM_001351032.2:c.-467-6318G=	NP_001337961.1:n.-467-6318G=
NM_020397.4:c.92+46874G=	NP_065130.1:n.92+46874G=
NM_153498.4:c.92+46874G= MANE Select	NP_705718.1:n.92+46874G=