Canonical Allele Identifier: CA410779172

Gene: LZTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20995873G>A , CM000684.2:g.20995873G>A	GRCh38
NC_000022.10:g.21350162G>A , CM000684.1:g.21350162G>A	GRCh37
NC_000022.9:g.19680162G>A	NCBI36
NG_034193.1:g.18605G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006767.4:c.2069+1G>A MANE Select	NP_006758.2:n.2069+1G>A
ENST00000646124.2:c.2069+1G>A MANE Select	ENSP00000496779.1:n.2069+1G>A
NM_006767.3:c.2069+1G>A	NP_006758.2:n.2069+1G>A
ENST00000215739.12:c.2069+1G>A	ENSP00000215739.8:n.2069+1G>A
ENST00000415354.6:c.498+1G>A	ENSP00000393765.2:n.498+1G>A
ENST00000415817.2:c.498+1G>A
ENST00000439171.5:c.468+1G>A
ENST00000452988.5:c.231+1G>A	ENSP00000408789.1:n.231+1G>A
ENST00000463909.1:n.784+1G>A
ENST00000479606.5:n.2215+1G>A
ENST00000491432.5:n.490+1G>A
ENST00000495142.5:n.685+1G>A
ENST00000495142.6:n.2421+1G>A
ENST00000498649.1:n.85+1G>A
ENST00000642151.1:c.1900+1G>A
ENST00000643578.1:n.2091+1G>A
ENST00000643710.1:n.930+1G>A
ENST00000646506.1:n.1936+1G>A
ENST00000700578.1:c.2069+1G>A	ENSP00000515073.1:n.2069+1G>A