Canonical Allele Identifier: CA2684804382

Gene: CALU

Linked Data

• gnomAD v4: 7-128759179-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128759179G>T , CM000669.2:g.128759179G>T	GRCh38
NC_000007.13:g.128399233G>T , CM000669.1:g.128399233G>T	GRCh37
NC_000007.12:g.128186469G>T	NCBI36
NG_033110.1:g.24888G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449187.7:c.582+142G>T	ENSP00000408838.2:n.582+142G>T
ENST00000542996.7:c.606+142G>T	ENSP00000438248.1:n.606+142G>T
ENST00000249364.9:c.582+142G>T MANE Select	ENSP00000249364.4:n.582+142G>T
ENST00000249364.8:c.582+142G>T	ENSP00000249364.4:n.582+142G>T
ENST00000449187.6:c.582+142G>T	ENSP00000408838.2:n.582+142G>T
ENST00000479257.5:c.606+142G>T	ENSP00000420381.1:n.606+142G>T
ENST00000493278.1:c.76+142G>T
ENST00000535011.6:c.582+142G>T	ENSP00000442110.1:n.582+142G>T
ENST00000542996.6:c.606+142G>T	ENSP00000438248.1:n.606+142G>T
NM_001130674.2:c.582+142G>T	NP_001124146.1:n.582+142G>T
NM_001199671.1:c.606+142G>T	NP_001186600.1:n.606+142G>T
NM_001199672.1:c.606+142G>T	NP_001186601.1:n.606+142G>T
NM_001199673.1:c.582+142G>T	NP_001186602.1:n.582+142G>T
NM_001219.4:c.582+142G>T	NP_001210.1:n.582+142G>T
NR_074086.1:n.308+142G>T
XM_011516588.1:c.360+142G>T	XP_011514890.1:n.360+142G>T
XM_017012659.1:c.129+142G>T	XP_016868148.1:n.129+142G>T
NM_001219.5:c.582+142G>T MANE Select	NP_001210.1:n.582+142G>T
NM_001130674.3:c.582+142G>T	NP_001124146.1:n.582+142G>T
NM_001199671.2:c.606+142G>T	NP_001186600.1:n.606+142G>T
NM_001199672.2:c.606+142G>T	NP_001186601.1:n.606+142G>T
NM_001199673.2:c.582+142G>T	NP_001186602.1:n.582+142G>T
NR_074086.2:n.241+142G>T