Canonical Allele Identifier: CA410780067
Community Standard Title: NM_006767.4(LZTR1):c.2219+2C>A
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20996114C>A , CM000684.2:g.20996114C>A GRCh38
NC_000022.10:g.21350403C>A , CM000684.1:g.21350403C>A GRCh37
NC_000022.9:g.19680403C>A NCBI36
NG_034193.1:g.18846C>A

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.2219+2C>A MANE Select NP_006758.2:n.2219+2C>A
ENST00000646124.2:c.2219+2C>A MANE Select ENSP00000496779.1:n.2219+2C>A
NM_006767.3:c.2219+2C>A NP_006758.2:n.2219+2C>A
ENST00000215739.12:c.2219+2C>A ENSP00000215739.8:n.2219+2C>A
ENST00000415817.1:c.117+2C>A
ENST00000415817.2:c.648+2C>A
ENST00000439171.5:c.618+2C>A
ENST00000452988.5:c.381+2C>A ENSP00000408789.1:n.381+2C>A
ENST00000463909.1:n.936C>A
ENST00000479606.5:n.2365+2C>A
ENST00000495142.6:n.2571+2C>A
ENST00000498649.1:n.235+2C>A
ENST00000642151.1:c.2050+2C>A
ENST00000643578.1:n.2241+2C>A
ENST00000643710.1:n.1080+2C>A
ENST00000646506.1:n.2086+2C>A
ENST00000700578.1:c.2219+2C>A ENSP00000515073.1:n.2219+2C>A