Canonical Allele Identifier: CA13181850

Gene: CAMK1D

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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