Canonical Allele Identifier: CA4472730

Gene: CALU

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128769067G>A , CM000669.2:g.128769067G>A	GRCh38
NC_000007.13:g.128409121G>A , CM000669.1:g.128409121G>A	GRCh37
NC_000007.12:g.128196357G>A	NCBI36
NG_033110.1:g.34776G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449187.7:c.848G>A	ENSP00000408838.2:p.Gly283Asp
ENST00000542996.7:c.872G>A	ENSP00000438248.1:p.Gly291Asp
ENST00000249364.9:c.848G>A MANE Select	ENSP00000249364.4:p.Gly283Asp
ENST00000249364.8:c.848G>A	ENSP00000249364.4:p.Gly283Asp
ENST00000449187.6:c.848G>A	ENSP00000408838.2:p.Gly283Asp
ENST00000479257.5:c.872G>A	ENSP00000420381.1:p.Gly291Asp
ENST00000493278.1:c.342G>A
ENST00000535011.6:c.648G>A	ENSP00000442110.1:p.Trp216Ter
ENST00000542996.6:c.872G>A	ENSP00000438248.1:p.Gly291Asp
NM_001130674.2:c.848G>A	NP_001124146.1:p.Gly283Asp
NM_001199671.1:c.872G>A	NP_001186600.1:p.Gly291Asp
NM_001199672.1:c.872G>A	NP_001186601.1:p.Gly291Asp
NM_001199673.1:c.648G>A	NP_001186602.1:p.Trp216Ter
NM_001219.4:c.848G>A	NP_001210.1:p.Gly283Asp
NR_074086.1:n.574G>A
XM_011516588.1:c.626G>A	XP_011514890.1:p.Gly209Asp
XM_017012659.1:c.395G>A	XP_016868148.1:p.Gly132Asp
NM_001219.5:c.848G>A MANE Select	NP_001210.1:p.Gly283Asp
NM_001130674.3:c.848G>A	NP_001124146.1:p.Gly283Asp
NM_001199671.2:c.872G>A	NP_001186600.1:p.Gly291Asp
NM_001199672.2:c.872G>A	NP_001186601.1:p.Gly291Asp
NM_001199673.2:c.648G>A	NP_001186602.1:p.Trp216Ter
NR_074086.2:n.507G>A