Canonical Allele Identifier: CA2518319864

Gene: CAMK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.12632966T>A , CM000672.2:g.12632966T>A	GRCh38
NC_000010.10:g.12674965T>A , CM000672.1:g.12674965T>A	GRCh37
NC_000010.9:g.12714971T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000619168.5:c.225-33770T>A MANE Select	ENSP00000478874.1:n.225-33770T>A
ENST00000378845.5:c.225-33770T>A	ENSP00000368122.1:n.225-33770T>A
ENST00000487696.1:n.260-33770T>A
ENST00000619168.4:c.225-33770T>A	ENSP00000478874.1:n.225-33770T>A
NM_020397.3:c.225-33770T>A	NP_065130.1:n.225-33770T>A
NM_153498.3:c.225-33770T>A	NP_705718.1:n.225-33770T>A
XM_006717481.2:c.168-33770T>A	XP_006717544.1:n.168-33770T>A
XM_006717482.2:c.225-33770T>A	XP_006717545.1:n.225-33770T>A
XM_006717483.2:c.225-33770T>A	XP_006717546.1:n.225-33770T>A
XM_011519591.1:c.186-33770T>A	XP_011517893.1:n.186-33770T>A
NM_001351032.1:c.-67-33770T>A	NP_001337961.1:n.-67-33770T>A
XM_006717482.3:c.225-33770T>A	XP_006717545.1:n.225-33770T>A
XM_006717483.4:c.225-33770T>A	XP_006717546.1:n.225-33770T>A
XM_011519591.3:c.186-33770T>A	XP_011517893.1:n.186-33770T>A
XM_017016438.2:c.-67-33770T>A	XP_016871927.1:n.-67-33770T>A
XM_024448087.1:c.-67-33770T>A	XP_024303855.1:n.-67-33770T>A
NM_001351032.2:c.-67-33770T>A	NP_001337961.1:n.-67-33770T>A
NM_020397.4:c.225-33770T>A	NP_065130.1:n.225-33770T>A
NM_153498.4:c.225-33770T>A MANE Select	NP_705718.1:n.225-33770T>A