Canonical Allele Identifier: CA10119111
Community Standard Title: NM_006767.4(LZTR1):c.1942+2T>C
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20995028T>C , CM000684.2:g.20995028T>C GRCh38
NC_000022.10:g.21349317T>C , CM000684.1:g.21349317T>C GRCh37
NC_000022.9:g.19679317T>C NCBI36
NG_034193.1:g.17760T>C

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.1942+2T>C MANE Select NP_006758.2:n.1942+2T>C
ENST00000646124.2:c.1942+2T>C MANE Select ENSP00000496779.1:n.1942+2T>C
NM_006767.3:c.1942+2T>C NP_006758.2:n.1942+2T>C
ENST00000215739.12:c.1942+2T>C ENSP00000215739.8:n.1942+2T>C
ENST00000415354.6:c.254+2T>C ENSP00000393765.2:n.254+2T>C
ENST00000415817.2:c.254+2T>C
ENST00000439171.5:c.224+2T>C
ENST00000452988.5:c.121+2T>C ENSP00000408789.1:n.121+2T>C
ENST00000464807.1:n.205T>C
ENST00000479606.5:n.2088+2T>C
ENST00000491432.5:n.363+2T>C
ENST00000495142.5:n.558+2T>C
ENST00000495142.6:n.1577T>C
ENST00000642151.1:c.1773+2T>C
ENST00000643578.1:n.1964+2T>C
ENST00000643710.1:n.803+2T>C
ENST00000646506.1:n.1809+2T>C
ENST00000700578.1:c.1942+2T>C ENSP00000515073.1:n.1942+2T>C