Canonical Allele Identifier: CA2838450368

Gene: CAMK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.12763449T>C , CM000672.2:g.12763449T>C	GRCh38
NC_000010.10:g.12805448T>C , CM000672.1:g.12805448T>C	GRCh37
NC_000010.9:g.12845454T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619168.5:c.438+2363T>C MANE Select	ENSP00000478874.1:n.438+2363T>C
ENST00000378845.5:c.438+2363T>C	ENSP00000368122.1:n.438+2363T>C
ENST00000615792.1:c.156+2363T>C	ENSP00000478861.1:n.156+2363T>C
ENST00000619168.4:c.438+2363T>C	ENSP00000478874.1:n.438+2363T>C
NM_020397.3:c.438+2363T>C	NP_065130.1:n.438+2363T>C
NM_153498.3:c.438+2363T>C	NP_705718.1:n.438+2363T>C
XM_006717481.2:c.381+2363T>C	XP_006717544.1:n.381+2363T>C
XM_006717482.2:c.438+2363T>C	XP_006717545.1:n.438+2363T>C
XM_006717483.2:c.438+2363T>C	XP_006717546.1:n.438+2363T>C
XM_011519591.1:c.399+2363T>C	XP_011517893.1:n.399+2363T>C
XM_011519592.1:c.228+2363T>C	XP_011517894.1:n.228+2363T>C
XM_011519593.1:c.216+2363T>C	XP_011517895.1:n.216+2363T>C
XM_011519594.1:c.27+2363T>C	XP_011517896.1:n.27+2363T>C
XM_011519595.1:c.147+2363T>C	XP_011517897.1:n.147+2363T>C
XM_011519596.1:c.147+2363T>C	XP_011517898.1:n.147+2363T>C
NM_001351032.1:c.147+2363T>C	NP_001337961.1:n.147+2363T>C
XM_006717482.3:c.438+2363T>C	XP_006717545.1:n.438+2363T>C
XM_006717483.4:c.438+2363T>C	XP_006717546.1:n.438+2363T>C
XM_011519591.3:c.399+2363T>C	XP_011517893.1:n.399+2363T>C
XM_011519592.3:c.228+2363T>C	XP_011517894.1:n.228+2363T>C
XM_011519593.3:c.216+2363T>C	XP_011517895.1:n.216+2363T>C
XM_011519594.3:c.27+2363T>C	XP_011517896.1:n.27+2363T>C
XM_011519595.3:c.147+2363T>C	XP_011517897.1:n.147+2363T>C
XM_017016438.2:c.147+2363T>C	XP_016871927.1:n.147+2363T>C
XM_024448087.1:c.147+2363T>C	XP_024303855.1:n.147+2363T>C
NM_001351032.2:c.147+2363T>C	NP_001337961.1:n.147+2363T>C
NM_020397.4:c.438+2363T>C	NP_065130.1:n.438+2363T>C
NM_153498.4:c.438+2363T>C MANE Select	NP_705718.1:n.438+2363T>C