Canonical Allele Identifier: CA10118579
Community Standard Title: NM_006767.4(LZTR1):c.652-10C>A
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20990376C>A , CM000684.2:g.20990376C>A GRCh38
NC_000022.10:g.21344665C>A , CM000684.1:g.21344665C>A GRCh37
NC_000022.9:g.19674665C>A NCBI36
NG_034193.1:g.13108C>A

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.652-10C>A MANE Select NP_006758.2:n.652-10C>A
ENST00000646124.2:c.652-10C>A MANE Select ENSP00000496779.1:n.652-10C>A
NM_006767.3:c.652-10C>A NP_006758.2:n.652-10C>A
ENST00000215739.12:c.652-10C>A ENSP00000215739.8:n.652-10C>A
ENST00000414985.5:c.*218-10C>A ENSP00000397247.1:n.*218-10C>A
ENST00000479606.5:n.798-10C>A
ENST00000480895.1:n.348-10C>A
ENST00000497716.5:n.35-10C>A
ENST00000642151.1:c.483-10C>A
ENST00000644435.1:c.474-10C>A
ENST00000646506.1:n.231-10C>A
ENST00000700578.1:c.652-10C>A ENSP00000515073.1:n.652-10C>A