Canonical Allele Identifier: CA2579106898

Gene: LZTS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20253614A>C , CM000670.2:g.20253614A>C	GRCh38
NC_000008.10:g.20111125A>C , CM000670.1:g.20111125A>C	GRCh37
NC_000008.9:g.20155405A>C	NCBI36
NG_015834.2:g.6679T>G
NG_015834.3:g.55368T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265801.6:c.346-29T>G	ENSP00000265801.6:n.346-29T>G
ENST00000381569.5:c.346-29T>G MANE Select	ENSP00000370981.1:n.346-29T>G
ENST00000522290.5:c.346-29T>G	ENSP00000429263.1:n.346-29T>G
ENST00000616228.1:c.157+1411T>G	ENSP00000479534.1:n.157+1411T>G
NM_021020.3:c.346-29T>G	NP_066300.1:n.346-29T>G
XM_005273394.3:c.346-29T>G	XP_005273451.1:n.346-29T>G
XM_011544383.1:c.346-29T>G	XP_011542685.1:n.346-29T>G
XM_011544384.1:c.346-29T>G	XP_011542686.1:n.346-29T>G
XM_011544385.1:c.346-29T>G	XP_011542687.1:n.346-29T>G
XM_011544386.1:c.346-29T>G	XP_011542688.1:n.346-29T>G
XM_011544387.1:c.346-29T>G	XP_011542689.1:n.346-29T>G
NM_001362884.1:c.346-29T>G	NP_001349813.1:n.346-29T>G
NM_021020.4:c.346-29T>G	NP_066300.1:n.346-29T>G
XM_011544384.2:c.346-29T>G	XP_011542686.1:n.346-29T>G
XM_011544385.2:c.346-29T>G	XP_011542687.1:n.346-29T>G
XM_011544386.2:c.346-29T>G	XP_011542688.1:n.346-29T>G
NM_021020.5:c.346-29T>G MANE Select	NP_066300.1:n.346-29T>G
NM_001362884.2:c.346-29T>G	NP_001349813.1:n.346-29T>G