Canonical Allele Identifier: CA1958704142

Gene: LUZP2

Linked Data

• dbSNP Id: rs1850181954

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.24816301A>G , CM000673.2:g.24816301A>G	GRCh38
NC_000011.9:g.24837847A>G , CM000673.1:g.24837847A>G	GRCh37
NC_000011.8:g.24794423A>G	NCBI36
NG_030588.1:g.324332A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336930.11:c.396+52993A>G MANE Select	ENSP00000336817.6:n.396+52993A>G
ENST00000336930.10:c.396+52993A>G	ENSP00000336817.6:n.396+52993A>G
ENST00000405855.6:n.502-15603A>G
ENST00000529015.5:c.396+52993A>G	ENSP00000437032.1:n.396+52993A>G
ENST00000531187.5:n.670+52993A>G
ENST00000533227.5:c.138+52993A>G	ENSP00000432952.1:n.138+52993A>G
ENST00000620308.1:c.138+52993A>G	ENSP00000480441.1:n.138+52993A>G
NM_001009909.3:c.396+52993A>G	NP_001009909.2:n.396+52993A>G
NM_001252008.1:c.138+52993A>G	NP_001238937.1:n.138+52993A>G
NM_001252010.1:c.396+52993A>G	NP_001238939.1:n.396+52993A>G
XM_011520054.1:c.774+52993A>G	XP_011518356.1:n.774+52993A>G
XM_011520055.1:c.774+52993A>G	XP_011518357.1:n.774+52993A>G
XM_011520056.1:c.774+52993A>G	XP_011518358.1:n.774+52993A>G
XM_011520057.1:c.774+52993A>G	XP_011518359.1:n.774+52993A>G
XR_930864.1:n.1148+52993A>G
XM_011520056.3:c.774+52993A>G	XP_011518358.1:n.774+52993A>G
XM_017017648.2:c.774+52993A>G	XP_016873137.2:n.774+52993A>G
XM_017017649.2:c.774+52993A>G	XP_016873138.2:n.774+52993A>G
XM_024448468.1:c.774+52993A>G	XP_024304236.1:n.774+52993A>G
XR_930864.3:n.1148+52993A>G
NM_001009909.4:c.396+52993A>G MANE Select	NP_001009909.2:n.396+52993A>G
NM_001252008.2:c.138+52993A>G	NP_001238937.1:n.138+52993A>G
NM_001252010.2:c.396+52993A>G	NP_001238939.1:n.396+52993A>G