Canonical Allele Identifier: CA580946648

Gene: LZTS1

Linked Data

• dbSNP Id: rs1314371182
• gnomAD v2: 8-20111112-A-G
• gnomAD v4: 8-20253601-A-G
• MyVariant Identifiers: chr8:g.20111112A>G (hg19) ; chr8:g.20253601A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20253601A>G , CM000670.2:g.20253601A>G	GRCh38
NC_000008.10:g.20111112A>G , CM000670.1:g.20111112A>G	GRCh37
NC_000008.9:g.20155392A>G	NCBI36
NG_015834.2:g.6692T>C
NG_015834.3:g.55381T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265801.6:c.346-16T>C	ENSP00000265801.6:n.346-16T>C
ENST00000381569.5:c.346-16T>C MANE Select	ENSP00000370981.1:n.346-16T>C
ENST00000522290.5:c.346-16T>C	ENSP00000429263.1:n.346-16T>C
ENST00000616228.1:c.157+1424T>C	ENSP00000479534.1:n.157+1424T>C
NM_021020.3:c.346-16T>C	NP_066300.1:n.346-16T>C
XM_005273394.3:c.346-16T>C	XP_005273451.1:n.346-16T>C
XM_011544383.1:c.346-16T>C	XP_011542685.1:n.346-16T>C
XM_011544384.1:c.346-16T>C	XP_011542686.1:n.346-16T>C
XM_011544385.1:c.346-16T>C	XP_011542687.1:n.346-16T>C
XM_011544386.1:c.346-16T>C	XP_011542688.1:n.346-16T>C
XM_011544387.1:c.346-16T>C	XP_011542689.1:n.346-16T>C
NM_001362884.1:c.346-16T>C	NP_001349813.1:n.346-16T>C
NM_021020.4:c.346-16T>C	NP_066300.1:n.346-16T>C
XM_011544384.2:c.346-16T>C	XP_011542686.1:n.346-16T>C
XM_011544385.2:c.346-16T>C	XP_011542687.1:n.346-16T>C
XM_011544386.2:c.346-16T>C	XP_011542688.1:n.346-16T>C
NM_021020.5:c.346-16T>C MANE Select	NP_066300.1:n.346-16T>C
NM_001362884.2:c.346-16T>C	NP_001349813.1:n.346-16T>C