Canonical Allele Identifier: CA2684804399

Gene: CALU

Linked Data

• gnomAD v4: 7-128759187-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128759187T>G , CM000669.2:g.128759187T>G	GRCh38
NC_000007.13:g.128399241T>G , CM000669.1:g.128399241T>G	GRCh37
NC_000007.12:g.128186477T>G	NCBI36
NG_033110.1:g.24896T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449187.7:c.582+150T>G	ENSP00000408838.2:n.582+150T>G
ENST00000542996.7:c.606+150T>G	ENSP00000438248.1:n.606+150T>G
ENST00000249364.9:c.582+150T>G MANE Select	ENSP00000249364.4:n.582+150T>G
ENST00000249364.8:c.582+150T>G	ENSP00000249364.4:n.582+150T>G
ENST00000449187.6:c.582+150T>G	ENSP00000408838.2:n.582+150T>G
ENST00000479257.5:c.606+150T>G	ENSP00000420381.1:n.606+150T>G
ENST00000493278.1:c.76+150T>G
ENST00000535011.6:c.582+150T>G	ENSP00000442110.1:n.582+150T>G
ENST00000542996.6:c.606+150T>G	ENSP00000438248.1:n.606+150T>G
NM_001130674.2:c.582+150T>G	NP_001124146.1:n.582+150T>G
NM_001199671.1:c.606+150T>G	NP_001186600.1:n.606+150T>G
NM_001199672.1:c.606+150T>G	NP_001186601.1:n.606+150T>G
NM_001199673.1:c.582+150T>G	NP_001186602.1:n.582+150T>G
NM_001219.4:c.582+150T>G	NP_001210.1:n.582+150T>G
NR_074086.1:n.308+150T>G
XM_011516588.1:c.360+150T>G	XP_011514890.1:n.360+150T>G
XM_017012659.1:c.129+150T>G	XP_016868148.1:n.129+150T>G
NM_001219.5:c.582+150T>G MANE Select	NP_001210.1:n.582+150T>G
NM_001130674.3:c.582+150T>G	NP_001124146.1:n.582+150T>G
NM_001199671.2:c.606+150T>G	NP_001186600.1:n.606+150T>G
NM_001199672.2:c.606+150T>G	NP_001186601.1:n.606+150T>G
NM_001199673.2:c.582+150T>G	NP_001186602.1:n.582+150T>G
NR_074086.2:n.241+150T>G