Canonical Allele Identifier: CA1891316075

Gene: CAMK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.12833208C= , CM000672.2:g.12833208C=	GRCh38
NC_000010.10:g.12875208C= , CM000672.1:g.12875208C=	GRCh37
NC_000010.9:g.12915214C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_153498.4:c.*4321C= MANE Select	NP_705718.1:n.*4321C=
ENST00000619168.5:c.*4321C= MANE Select	ENSP00000478874.1:n.*4321C=
NM_153498.3:c.*4321C=	NP_705718.1:n.*4321C=
ENST00000619168.4:c.*4321C=	ENSP00000478874.1:n.*4321C=
XM_006717481.2:c.*4321C=	XP_006717544.1:n.*4321C=
XM_006717482.2:c.*4347C=	XP_006717545.1:n.*4347C=
XM_006717482.3:c.*4347C=	XP_006717545.1:n.*4347C=
XM_006717483.2:c.*4415C=	XP_006717546.1:n.*4415C=
XM_011519591.1:c.*4321C=	XP_011517893.1:n.*4321C=
XM_011519592.1:c.*4321C=	XP_011517894.1:n.*4321C=
XM_011519593.1:c.*4321C=	XP_011517895.1:n.*4321C=
XM_011519594.1:c.*4321C=	XP_011517896.1:n.*4321C=
XM_011519595.1:c.*4321C=	XP_011517897.1:n.*4321C=
XM_011519596.1:c.*4321C=	XP_011517898.1:n.*4321C=