Canonical Allele Identifier: CA13181994

Gene: CAMK1D

Linked Data

• dbSNP Id: rs7897059
• gnomAD v2: 10-12591712-C-T
• gnomAD v3: 10-12549713-C-T
• gnomAD v4: 10-12549713-C-T
• MyVariant Identifiers: chr10:g.12591712C>T (hg19) ; chr10:g.12549713C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.12549713C>T , CM000672.2:g.12549713C>T	GRCh38
NC_000010.10:g.12591712C>T , CM000672.1:g.12591712C>T	GRCh37
NC_000010.9:g.12631718C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000619168.5:c.93-3512C>T MANE Select	ENSP00000478874.1:n.93-3512C>T
ENST00000378845.5:c.93-3512C>T	ENSP00000368122.1:n.93-3512C>T
ENST00000487696.1:n.260-117023C>T
ENST00000619168.4:c.93-3512C>T	ENSP00000478874.1:n.93-3512C>T
NM_020397.3:c.93-3512C>T	NP_065130.1:n.93-3512C>T
NM_153498.3:c.93-3512C>T	NP_705718.1:n.93-3512C>T
XM_006717481.2:c.36-3512C>T	XP_006717544.1:n.36-3512C>T
XM_006717482.2:c.93-3512C>T	XP_006717545.1:n.93-3512C>T
XM_006717483.2:c.93-3512C>T	XP_006717546.1:n.93-3512C>T
XM_011519591.1:c.54-3512C>T	XP_011517893.1:n.54-3512C>T
NM_001351032.1:c.-199-3512C>T	NP_001337961.1:n.-199-3512C>T
XM_006717482.3:c.93-3512C>T	XP_006717545.1:n.93-3512C>T
XM_006717483.4:c.93-3512C>T	XP_006717546.1:n.93-3512C>T
XM_011519591.3:c.54-3512C>T	XP_011517893.1:n.54-3512C>T
XM_017016438.2:c.-199-3512C>T	XP_016871927.1:n.-199-3512C>T
XM_024448087.1:c.-199-3512C>T	XP_024303855.1:n.-199-3512C>T
NM_001351032.2:c.-199-3512C>T	NP_001337961.1:n.-199-3512C>T
NM_020397.4:c.93-3512C>T	NP_065130.1:n.93-3512C>T
NM_153498.4:c.93-3512C>T MANE Select	NP_705718.1:n.93-3512C>T