Canonical Allele Identifier: CA1342394
Gene: LAX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203771422C>A , CM000663.2:g.203771422C>A GRCh38
NC_000001.10:g.203740550C>A , CM000663.1:g.203740550C>A GRCh37
NC_000001.9:g.202007173C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000442561.7:c.255C>A MANE Select ENSP00000406970.2:p.Thr85=
ENST00000367215.1:n.225C>A
ENST00000367217.5:c.207C>A ENSP00000356186.5:p.Thr69=
ENST00000442561.6:c.255C>A ENSP00000406970.2:p.Thr85=
NM_001136190.1:c.207C>A NP_001129662.1:p.Thr69=
NM_001282878.1:c.27C>A NP_001269807.1:p.Thr9=
NM_017773.3:c.255C>A NP_060243.2:p.Thr85=
XM_006711397.2:c.255C>A XP_006711460.1:p.Thr85=
XM_006711397.3:c.255C>A XP_006711460.1:p.Thr85=
NM_001136190.2:c.207C>A NP_001129662.1:p.Thr69=
NM_017773.4:c.255C>A MANE Select NP_060243.2:p.Thr85=