Canonical Allele Identifier: CA1891114553

Gene: CAMK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.12393380C= , CM000672.2:g.12393380C=	GRCh38
NC_000010.10:g.12435379C= , CM000672.1:g.12435379C=	GRCh37
NC_000010.9:g.12475385C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_153498.4:c.92+43470C= MANE Select	NP_705718.1:n.92+43470C=
ENST00000619168.5:c.92+43470C= MANE Select	ENSP00000478874.1:n.92+43470C=
NM_001351032.1:c.-468+3381C=	NP_001337961.1:n.-468+3381C=
NM_001351032.2:c.-468+3381C=	NP_001337961.1:n.-468+3381C=
NM_020397.3:c.92+43470C=	NP_065130.1:n.92+43470C=
NM_020397.4:c.92+43470C=	NP_065130.1:n.92+43470C=
NM_153498.3:c.92+43470C=	NP_705718.1:n.92+43470C=
ENST00000378845.5:c.92+43470C=	ENSP00000368122.1:n.92+43470C=
ENST00000487696.1:n.259+43470C=
ENST00000619168.4:c.92+43470C=	ENSP00000478874.1:n.92+43470C=
XM_006717482.2:c.92+43470C=	XP_006717545.1:n.92+43470C=
XM_006717482.3:c.92+43470C=	XP_006717545.1:n.92+43470C=
XM_006717483.2:c.92+43470C=	XP_006717546.1:n.92+43470C=
XM_006717483.4:c.92+43470C=	XP_006717546.1:n.92+43470C=
XM_011519591.1:c.53+4323C=	XP_011517893.1:n.53+4323C=
XM_011519591.3:c.53+4323C=	XP_011517893.1:n.53+4323C=
XM_017016438.2:c.-467-9722C=	XP_016871927.1:n.-467-9722C=
XM_024448087.1:c.-468+3381C=	XP_024303855.1:n.-468+3381C=