Canonical Allele Identifier: CA1958704066

Gene: LUZP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.24816168_24816169delinsCT , CM000673.2:g.24816168_24816169delinsCT	GRCh38
NC_000011.9:g.24837714_24837715delinsCT , CM000673.1:g.24837714_24837715delinsCT	GRCh37
NC_000011.8:g.24794290_24794291delinsCT	NCBI36
NG_030588.1:g.324199_324200delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000336930.11:c.396+52860_396+52861delinsCT MANE Select	ENSP00000336817.6:n.396+52860_396+52861de...
ENST00000336930.10:c.396+52860_396+52861delinsCT	ENSP00000336817.6:n.396+52860_396+52861de...
ENST00000405855.6:n.502-15736_502-15735delinsCT
ENST00000529015.5:c.396+52860_396+52861delinsCT	ENSP00000437032.1:n.396+52860_396+52861de...
ENST00000531187.5:n.670+52860_670+52861delinsCT
ENST00000533227.5:c.138+52860_138+52861delinsCT	ENSP00000432952.1:n.138+52860_138+52861de...
ENST00000620308.1:c.138+52860_138+52861delinsCT	ENSP00000480441.1:n.138+52860_138+52861de...
NM_001009909.3:c.396+52860_396+52861delinsCT	NP_001009909.2:n.396+52860_396+52861delin...
NM_001252008.1:c.138+52860_138+52861delinsCT	NP_001238937.1:n.138+52860_138+52861delin...
NM_001252010.1:c.396+52860_396+52861delinsCT	NP_001238939.1:n.396+52860_396+52861delin...
XM_011520054.1:c.774+52860_774+52861delinsCT	XP_011518356.1:n.774+52860_774+52861delin...
XM_011520055.1:c.774+52860_774+52861delinsCT	XP_011518357.1:n.774+52860_774+52861delin...
XM_011520056.1:c.774+52860_774+52861delinsCT	XP_011518358.1:n.774+52860_774+52861delin...
XM_011520057.1:c.774+52860_774+52861delinsCT	XP_011518359.1:n.774+52860_774+52861delin...
XR_930864.1:n.1148+52860_1148+52861delinsCT
XM_011520056.3:c.774+52860_774+52861delinsCT	XP_011518358.1:n.774+52860_774+52861delin...
XM_017017648.2:c.774+52860_774+52861delinsCT	XP_016873137.2:n.774+52860_774+52861delin...
XM_017017649.2:c.774+52860_774+52861delinsCT	XP_016873138.2:n.774+52860_774+52861delin...
XM_024448468.1:c.774+52860_774+52861delinsCT	XP_024304236.1:n.774+52860_774+52861delin...
XR_930864.3:n.1148+52860_1148+52861delinsCT
NM_001009909.4:c.396+52860_396+52861delinsCT MANE Select	NP_001009909.2:n.396+52860_396+52861delin...
NM_001252008.2:c.138+52860_138+52861delinsCT	NP_001238937.1:n.138+52860_138+52861delin...
NM_001252010.2:c.396+52860_396+52861delinsCT	NP_001238939.1:n.396+52860_396+52861delin...