Canonical Allele Identifier: CA410779953

Gene: LZTR1

Linked Data

• ClinVar Variation Id: 522799
• ClinVar RCV Id: RCV000625963 ; RCV003162767 ; RCV002533148
• dbSNP Id: rs1034395178
• gnomAD v2: 22-21350360-C-A
• gnomAD v4: 22-20996071-C-A
• MyVariant Identifiers: chr22:g.21350360C>A (hg19) ; chr22:g.20996071C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20996071C>A , CM000684.2:g.20996071C>A	GRCh38
NC_000022.10:g.21350360C>A , CM000684.1:g.21350360C>A	GRCh37
NC_000022.9:g.19680360C>A	NCBI36
NG_034193.1:g.18803C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700578.1:c.2178C>A	ENSP00000515073.1:p.Tyr726Ter
ENST00000415817.2:c.607C>A
ENST00000495142.6:n.2530C>A
ENST00000642151.1:c.2009C>A
ENST00000643578.1:n.2200C>A
ENST00000643710.1:n.1039C>A
ENST00000646124.2:c.2178C>A MANE Select	ENSP00000496779.1:p.Tyr726Ter
ENST00000646506.1:n.2045C>A
ENST00000215739.12:c.2178C>A	ENSP00000215739.8:p.Tyr726Ter
ENST00000415354.6:c.607C>A	ENSP00000393765.2:n.607C>A
ENST00000415817.1:c.76C>A
ENST00000439171.5:c.577C>A
ENST00000452988.5:c.340C>A	ENSP00000408789.1:n.340C>A
ENST00000463909.1:n.893C>A
ENST00000479606.5:n.2324C>A
ENST00000498649.1:n.194C>A
NM_006767.3:c.2178C>A	NP_006758.2:p.Tyr726Ter
NM_006767.4:c.2178C>A MANE Select	NP_006758.2:p.Tyr726Ter