Canonical Allele Identifier: CA459880691

Gene: LZTS1

Linked Data

• gnomAD v4: 8-20253580-G-T
• MyVariant Identifiers: chr8:g.20111091G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20253580G>T , CM000670.2:g.20253580G>T	GRCh38
NC_000008.10:g.20111091G>T , CM000670.1:g.20111091G>T	GRCh37
NC_000008.9:g.20155371G>T	NCBI36
NG_015834.2:g.6713C>A
NG_015834.3:g.55402C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265801.6:c.351C>A	ENSP00000265801.6:p.Ser117=
ENST00000381569.5:c.351C>A MANE Select	ENSP00000370981.1:p.Ser117=
ENST00000522290.5:c.351C>A	ENSP00000429263.1:p.Ser117=
ENST00000616228.1:c.157+1445C>A	ENSP00000479534.1:n.157+1445C>A
NM_021020.3:c.351C>A	NP_066300.1:p.Ser117=
XM_005273394.3:c.351C>A	XP_005273451.1:p.Ser117=
XM_011544383.1:c.351C>A	XP_011542685.1:p.Ser117=
XM_011544384.1:c.351C>A	XP_011542686.1:p.Ser117=
XM_011544385.1:c.351C>A	XP_011542687.1:p.Ser117=
XM_011544386.1:c.351C>A	XP_011542688.1:p.Ser117=
XM_011544387.1:c.351C>A	XP_011542689.1:p.Ser117=
NM_001362884.1:c.351C>A	NP_001349813.1:p.Ser117=
NM_021020.4:c.351C>A	NP_066300.1:p.Ser117=
XM_011544384.2:c.351C>A	XP_011542686.1:p.Ser117=
XM_011544385.2:c.351C>A	XP_011542687.1:p.Ser117=
XM_011544386.2:c.351C>A	XP_011542688.1:p.Ser117=
NM_021020.5:c.351C>A MANE Select	NP_066300.1:p.Ser117=
NM_001362884.2:c.351C>A	NP_001349813.1:p.Ser117=