Canonical Allele Identifier: CA410776306
Community Standard Title: NM_006767.4(LZTR1):c.1615+2T>C
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20994271T>C , CM000684.2:g.20994271T>C GRCh38
NC_000022.10:g.21348560T>C , CM000684.1:g.21348560T>C GRCh37
NC_000022.9:g.19678560T>C NCBI36
NG_034193.1:g.17003T>C

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.1615+2T>C MANE Select NP_006758.2:n.1615+2T>C
ENST00000646124.2:c.1615+2T>C MANE Select ENSP00000496779.1:n.1615+2T>C
NM_006767.3:c.1615+2T>C NP_006758.2:n.1615+2T>C
ENST00000215739.12:c.1615+2T>C ENSP00000215739.8:n.1615+2T>C
ENST00000415354.6:c.43+2T>C ENSP00000393765.2:n.43+2T>C
ENST00000479606.5:n.1761+2T>C
ENST00000492480.1:n.666T>C
ENST00000495142.6:n.962T>C
ENST00000642151.1:c.1446+2T>C
ENST00000643578.1:n.1637+2T>C
ENST00000643710.1:n.476+2T>C
ENST00000646506.1:n.1196T>C
ENST00000700578.1:c.1615+2T>C ENSP00000515073.1:n.1615+2T>C