Canonical Allele Identifier: CA16043174
Gene: LZTR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 373302
ClinVar RCV Id: RCV000413376
dbSNP Id: rs1057518336

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20990471A>C , CM000684.2:g.20990471A>C GRCh38
NC_000022.10:g.21344760A>C , CM000684.1:g.21344760A>C GRCh37
NC_000022.9:g.19674760A>C NCBI36
NG_034193.1:g.13203A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000700578.1:c.737A>C ENSP00000515073.1:p.Gln246Pro
ENST00000642151.1:c.568A>C
ENST00000644435.1:c.559A>C
ENST00000646124.2:c.737A>C MANE Select ENSP00000496779.1:p.Gln246Pro
ENST00000646506.1:n.316A>C
ENST00000215739.12:c.737A>C ENSP00000215739.8:p.Gln246Pro
ENST00000414985.5:c.*303A>C ENSP00000397247.1:n.*303A>C
ENST00000479606.5:n.883A>C
ENST00000480895.1:n.433A>C
ENST00000497716.5:n.120A>C
NM_006767.3:c.737A>C NP_006758.2:p.Gln246Pro
NM_006767.4:c.737A>C MANE Select NP_006758.2:p.Gln246Pro